Old Web
English
Sign In
Acemap
>
Paper
>
Crouzon syndrome and Bent bone dysplasia associated with mutations at the same Tyr‐381 residue in FGFR2 gene
Crouzon syndrome and Bent bone dysplasia associated with mutations at the same Tyr‐381 residue in FGFR2 gene
2014
Corinne Collet
Jean-Luc Alessandri
E. Arnaud
M. Balu
V. C. Daire
F. Di Rocco
Keywords:
Internal medicine
Missense mutation
Tyrosine
Endocrinology
Gene
Fibroblast growth factor
Asparagine
Biology
Molecular biology
Receptor
Crouzon syndrome
Mutation
Correction
Source
Cite
Save
Machine Reading By IdeaReader
6
References
6
Citations
NaN
KQI
[]