Two common mutations 934C to G and 937C to G of fibroblast growth factor receptor 2 (FGFR2) gene in Chinese patients with Apert syndrome.

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Tsai FJ, Hwu WL, Lin SP, Chang JG, Wang TR, Tsai CH

Two common mutations 934C to G and 937C to G of fibroblast growth factor receptor 2 (FGFR2) gene in Chinese patients with Apert syndrome.

Hum Mutat. 1998;Suppl 1:S18-9.

PubMed ID
9452027 [ View in PubMed
]
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DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Fibroblast growth factor receptor 2P21802Details