| DISEASE | TITLE OF PUBLICATION | LINK TO PUBMED |
| Charcot-Marie-Tooth Disease | A French family with Charcot-Marie-Tooth disease related to simultaneous heterozygous MFN2 and GDAP1 mutations. |  PubMed |
| Charcot-Marie-Tooth Disease | A novel autosomal dominant GDAP1 mutation in an Italian CMT2 family. | PubMed |
| Charcot-Marie-Tooth Disease | A novel GDAP1 Q218E mutation in autosomal dominant Charcot-Marie-Tooth disease. | PubMed |
| Charcot-Marie-Tooth Disease | A novel mutation in the GDAP1 gene is associated with autosomal recessive Charcot-Marie-Tooth disease in an Amish family. | PubMed |
| Charcot-Marie-Tooth Disease | A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effect. | PubMed |
| Charcot-Marie-Tooth Disease | Autosomal recessive axonal form of Charcot-Marie-Tooth Disease caused by compound heterozygous 3'-splice site and Ser130Cys mutation in the GDAP1 gene. | PubMed |
| Charcot-Marie-Tooth Disease | Charcot-Marie-Tooth disease CMT4A: GDAP1 increases cellular glutathione and the mitochondrial membrane potential. | PubMed |
| Charcot-Marie-Tooth Disease | Charcot-Marie-Tooth disease type 4C4 caused by a novel Pro153Leu substitution in the GDAP1 gene. | PubMed |
| Charcot-Marie-Tooth Disease | Charcot-Marie-Tooth-related gene GDAP1 complements cell cycle delay at G2/M phase in Saccharomyces cerevisiae fis1 gene-defective cells. | PubMed |
| Charcot-Marie-Tooth Disease | Early onset Charcot-Marie-Tooth disease caused by a homozygous Leu239Phe mutation in the GDAP1 gene. | PubMed |
| Charcot-Marie-Tooth Disease | Evolutionary and structural analyses of GDAP1, involved in Charcot-Marie-Tooth disease, characterize a novel class of glutathione transferase-related genes. | PubMed |
| Charcot-Marie-Tooth Disease | Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network: new implications for Charcot-Marie-Tooth disease. | PubMed |
| Charcot-Marie-Tooth Disease | GDAP1, the protein causing Charcot-Marie-Tooth disease type 4A, is expressed in neurons and is associated with mitochondria. | PubMed |
| Charcot-Marie-Tooth Disease | Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth disease. | PubMed |
| Charcot-Marie-Tooth Disease | L239F founder mutation in GDAP1 is associated with a mild Charcot-Marie-Tooth type 4C4 (CMT4C4) phenotype. | PubMed |
| Charcot-Marie-Tooth Disease | Mitochondrial complex I deficiency in GDAP1-related autosomal dominant Charcot-Marie-Tooth disease (CMT2K). | PubMed |
| Charcot-Marie-Tooth Disease | Mitochondrial dysfunction and pathophysiology of Charcot-Marie-Tooth disease involving GDAP1 mutations. | PubMed |
| Charcot-Marie-Tooth Disease | Novel human pathological mutations. Gene symbol: GDAP1. Disease: Charcot-Marie-Tooth disease 4A. | PubMed |
| Charcot-Marie-Tooth Disease | Phenotypical features of a Moroccan family with autosomal recessive Charcot-Marie-Tooth disease associated with the S194X mutation in the GDAP1 gene. | PubMed |
| Charcot-Marie-Tooth Disease | Phenotypical features of the p.R120W mutation in the GDAP1 gene causing autosomal dominant Charcot-Marie-Tooth disease. | PubMed |
| Charcot-Marie-Tooth Disease | Vocal cord and diaphragm paralysis, as clinical features of a French family with autosomal recessive Charcot-Marie-Tooth disease, associated with a new mutation in the GDAP1 gene. | PubMed |
| Charcot-Marie-Tooth Disease | YY1-dependent transcriptional regulation of the human GDAP1 gene. | PubMed |
| Clubfoot | Mutations in the ganglioside-induced differentiation-associated protein-1 (GDAP1) gene in intermediate type autosomal recessive Charcot-Marie-Tooth neuropathy. | PubMed |
| Congenital Abnormalities | Mutations in the ganglioside-induced differentiation-associated protein-1 (GDAP1) gene in intermediate type autosomal recessive Charcot-Marie-Tooth neuropathy. | PubMed |
| Demyelinating Diseases | A locus-specific database for mutations in GDAP1 allows analysis of genotype-phenotype correlations in Charcot-Marie-Tooth diseases type 4A and 2K. | PubMed |
| Demyelinating Diseases | Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network: new implications for Charcot-Marie-Tooth disease. | PubMed |
| Demyelinating Diseases | Mutations in GDAP1: autosomal recessive CMT with demyelination and axonopathy. | PubMed |
| Demyelinating Diseases | Mutations in the ganglioside-induced differentiation-associated protein-1 (GDAP1) gene in intermediate type autosomal recessive Charcot-Marie-Tooth neuropathy. | PubMed |
| Foot Deformities | Genetic spectrum of hereditary neuropathies with onset in the first year of life. | PubMed |
| Hereditary Sensory and Motor Neuropathy | Genetic study of demyelinating form of autosomal-recessive Charcot-Marie-tooth diseases in a Turkish family. | PubMed |
| Hereditary Sensory and Motor Neuropathy | [Molecular genetics of inherited neuropathies] | PubMed, PubMed |
| Hoarseness | Charcot-Marie-Tooth disease type 4C4 caused by a novel Pro153Leu substitution in the GDAP1 gene. | PubMed |
| Mitochondrial Diseases | A locus-specific database for mutations in GDAP1 allows analysis of genotype-phenotype correlations in Charcot-Marie-Tooth diseases type 4A and 2K. | PubMed |
| Muscle Weakness | Two novel mutations in the GDAP1 and PRX genes in early onset Charcot-Marie-Tooth syndrome. | PubMed |
| Neoplasms | ENTPD5, an Endoplasmic Reticulum UDPase, Alleviates ER Stress Induced by Protein Overloading in ATK-Activated Cancer Cells. | PubMed |
| Neoplasms | YY1-dependent transcriptional regulation of the human GDAP1 gene. | PubMed |
| Neuroblastoma | GDAP1, the protein causing Charcot-Marie-Tooth disease type 4A, is expressed in neurons and is associated with mitochondria. | PubMed |
| Neurodegenerative Diseases | Mitochondrial dysfunction and pathophysiology of Charcot-Marie-Tooth disease involving GDAP1 mutations. | PubMed |
| Ophthalmoplegia | Inherited mitochondrial neuropathies. | PubMed |
| Ovarian Neoplasms | Sialyltransferase and nucleoside diphosphatase as markers for tumor monitoring. | PubMed |
| Paralysis | Clinical, electrophysiological and morphological findings of Charcot-Marie-Tooth neuropathy with vocal cord palsy and mutations in the GDAP1 gene. | PubMed |
| Paralysis | Vocal cord and diaphragm paralysis, as clinical features of a French family with autosomal recessive Charcot-Marie-Tooth disease, associated with a new mutation in the GDAP1 gene. | PubMed |
| Paresis | The gene encoding ganglioside-induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A disease. | PubMed |
| Peripheral Nervous System Diseases | Cell expression of GDAP1 in the nervous system and pathogenesis of Charcot-Marie-Tooth type 4A disease. | PubMed |
| Peripheral Nervous System Diseases | Charcot-Marie-Tooth disease CMT4A: GDAP1 increases cellular glutathione and the mitochondrial membrane potential. | PubMed |
| Peripheral Nervous System Diseases | GDAP1 mutations differ in their effects on mitochondrial dynamics and apoptosis depending on the mode of inheritance. | PubMed |
| Peripheral Nervous System Diseases | Mitochondrial dysfunction and pathophysiology of Charcot-Marie-Tooth disease involving GDAP1 mutations. | PubMed |
| Polyneuropathies | Inherited mitochondrial neuropathies. | PubMed |
| Respiratory Insufficiency | Vocal cord paresis and diaphragmatic dysfunction are severe and frequent symptoms of GDAP1-associated neuropathy. | PubMed |
| Vocal Cord Paralysis | Clinical, electrophysiological and morphological findings of Charcot-Marie-Tooth neuropathy with vocal cord palsy and mutations in the GDAP1 gene. | PubMed |
| Vocal Cord Paralysis | The gene encoding ganglioside-induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A disease. | PubMed |
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