Crouzon syndrome: previously unrecognized deletion, duplication, and point mutation within FGFR2 gene.

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Steinberger D, Mulliken JB, Muller U

Crouzon syndrome: previously unrecognized deletion, duplication, and point mutation within FGFR2 gene.

Hum Mutat. 1996;8(4):386-90.

PubMed ID
8956050 [ View in PubMed
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DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Fibroblast growth factor receptor 2P21802Details