Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia

author
created [InstanceEdit:2060829] Rothfels, K, 2012-01-16
dbId 2060842
displayName Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia
journal Cell
modified [InstanceEdit:2060866] Rothfels, K, 2012-01-16
pages 335-42
pubMedIdentifier 7913883
schemaClass LiteratureReference
title Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia
url http://www.ncbi.nlm.nih.gov/pubmed/7913883
volume 78
year 1994
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