Glycine

fibroblast growth factor receptor 3 ; Homo sapiens







4 Article(s)
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PMID
Title
Pub. Year
#Total Relationships
1 17256796 Clinical hypochondroplasia in a family caused by a heterozygous double mutation in FGFR3 encoding GLY380LYS. 2007 Feb 15 2
2 9136983 Activation of FGF receptors by mutations in the transmembrane domain. 1997 Mar 27 1
3 8599935 Constitutive activation of fibroblast growth factor receptor 3 by the transmembrane domain point mutation found in achondroplasia. 1996 Feb 1 2
4 7913883 Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia. 1994 Jul 29 1