Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand

author
created [InstanceEdit:2029800] Rothfels, K, 2012-01-04
dbId 2029801
displayName Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand
journal Hum Mol Genet
pages 1475-83
pubMedIdentifier 9700203
schemaClass LiteratureReference
title Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand
url http://www.ncbi.nlm.nih.gov/pubmed/9700203
volume 7
year 1998
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