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Details on Person Trp290Cys mutation in exon IIIa of the fibroblast growth factor receptor 2 (FGFR2) gene is associated with Pfeiffer syndrome
| Class:Id | LiteratureReference:2060773 |
|---|---|
| _displayName | Trp290Cys mutation in exon IIIa of the fibroblast growth factor receptor 2 (FGFR2) gene is associated with Pfeiffer syndrome |
| _timestamp | 2012-01-16 04:18:40 |
| author | [Person:2060728] Tartaglia, M [Person:2060734] Valeri, S [Person:2060735] Velardi, F [Person:2060693] Di Rocco, C [Person:2060687] Battaglia, PA |
| created | [InstanceEdit:2060774] Rothfels, K, 2012-01-16 |
| journal | Hum Genet |
| pages | 602-6 |
| pubMedIdentifier | 9150725 |
| title | Trp290Cys mutation in exon IIIa of the fibroblast growth factor receptor 2 (FGFR2) gene is associated with Pfeiffer syndrome |
| volume | 99 |
| year | 1997 |
| (literatureReference) | [EntityWithAccessionedSequence:1637929] FGFR2 W290C [plasma membrane] [Homo sapiens] |
| [Change default viewing format] | |
No pathways have been reviewed or authored by Trp290Cys mutation in exon IIIa of the fibroblast growth factor receptor 2 (FGFR2) gene is associated with Pfeiffer syndrome (2060773)
