Distinct missense mutations of the FGFR3 lys650 codon modulate receptor kinase activation and the severity of the skeletal dysplasia phenotype

author
created [InstanceEdit:2032926] Rothfels, K, 2012-01-08
dbId 2032927
displayName Distinct missense mutations of the FGFR3 lys650 codon modulate receptor kinase activation and the severity of the skeletal dysplasia phenotype
journal Am J Hum Genet
pages 1411-21
pubMedIdentifier 11055896
schemaClass LiteratureReference
title Distinct missense mutations of the FGFR3 lys650 codon modulate receptor kinase activation and the severity of the skeletal dysplasia phenotype
url http://www.ncbi.nlm.nih.gov/pubmed/11055896
volume 67
year 2000

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