A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia

author
created [InstanceEdit:2054032] Rothfels, K, 2012-01-12
dbId 2054031
displayName A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia
journal Nat Genet
pages 357-9
pubMedIdentifier 7670477
schemaClass LiteratureReference
title A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia
url http://www.ncbi.nlm.nih.gov/pubmed/7670477
volume 10
year 1995
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