Literature summary for 2.7.10.1 extracted from

Wilkie, A.O.; Slaney, S.F.; Oldridge, M.; Poole, M.D.; Ashworth, G.J.; Hockley, A.D.; Hayward, R.D.; David, D.J.; Pulleyn, L.J.; Rutland, P.; et al.
Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome (1995), Nat. Genet., 9, 165-172.

Protein Variants

Protein Variants	Comment	Organism
additional information	Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome	Homo sapiens

Organism	UniProt	Comment	Textmining
Homo sapiens	P21802	-	-

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Release 2023.1 (January 2023)