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Literature summary for 2.7.10.1 extracted from

  • Steinberger, D.; Mulliken, J.B.; Muller, U.
    Crouzon syndrome: previously unrecognized deletion, duplication, and point mutation within FGFR2 gene (1996), Hum. Mutat., 8, 386-390.
    View publication on PubMed

Protein Variants

Protein Variants Comment Organism
additional information Crouzon syndrome: deletion, duplication, and point mutation within FGFR2 gene Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens P21802
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-

Synonyms

Synonyms Comment Organism
fibroblast growth factor receptor 2
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Homo sapiens