Literature summary for 2.7.10.1 extracted from

Rutland, P.; Pulleyn, L.J.; Reardon, W.; Baraitser, M.; Hayward, R.; Jones, B.; Malcolm, S.; Winter, R.M.; Oldridge, M.; Slaney, S.F.; et al.
Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes (1995), Nat. Genet., 9, 173-176.

Protein Variants

Protein Variants	Comment	Organism
additional information	identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes	Homo sapiens

Organism	UniProt	Comment	Textmining
Homo sapiens	P21802	-	-

Synonyms	Comment	Organism
fibroblast growth factor receptor 2	-	Homo sapiens

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Release 2023.1 (January 2023)