Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain.

Article Details

Citation

McGillivray G, Savarirayan R, Cox TC, Stojkoski C, McNeil R, Bankier A, Bateman JF, Roscioli T, Gardner RJ, Lamande SR

Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain.

J Med Genet. 2005 Aug;42(8):656-62.

PubMed ID
16061565 [ View in PubMed
]
Abstract

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DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Fibroblast growth factor receptor 2P21802Details