Literature summary for 1.3.5.1 extracted from

Villeneuve, N; Abidi, A; Cacciagli, P; Mignon-Ravix, C; Chabrol, B; Villard, L; Milh, M
Heterogeneity of FHF1 related phenotype: Novel case with early onset severe attacks of apnea, partial mitochondrial respiratory chain complex II deficiency, neonatal onset seizures without neurodegeneration. (2017), Eur J Paediatr Neurol, 21, 783-786.

Organism

Organism	UniProt	Comment	Textmining

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Release 2023.1 (January 2023)