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Details on Person A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia
| Class:Id | LiteratureReference:2054031 |
|---|---|
| _displayName | A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia |
| _timestamp | 2012-01-12 21:58:31 |
| author | [Person:2032804] Bellus, GA [Person:2032855] McIntosh, I [Person:2054013] Smith, EA [Person:2053975] Aylsworth, AS [Person:2053995] Kaitila, I [Person:2053991] Horton, WA [Person:2053984] Greenhaw, GA [Person:2053988] Hecht, JT [Person:2032819] Francomano, CA |
| created | [InstanceEdit:2054032] Rothfels, K, 2012-01-12 |
| journal | Nat Genet |
| pages | 357-9 |
| pubMedIdentifier | 7670477 |
| title | A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia |
| volume | 10 |
| year | 1995 |
| (literatureReference) | [Pathway:1839122] Signaling by activated point mutants of FGFR1 [Homo sapiens] [Pathway:5655332] Signaling by FGFR3 in disease [Homo sapiens] |
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No pathways have been reviewed or authored by A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia (2054031)
