Reactome | McIntosh, I

Schema > Person > Entries

created	[InstanceEdit:2032854] Rothfels, K, 2012-01-08
dbId	2032855
displayName	McIntosh, I
firstname	Iain
initial	I
publications	[LiteratureReference:2054031] A recurrent mutation in the tyrosine kinase domain of fibroblast growth factor receptor 3 causes hypochondroplasia [LiteratureReference:2032916] A novel skeletal dysplasia with developmental delay and acanthosis nigricans is caused by a Lys650Met mutation in the fibroblast growth factor receptor 3 gene [LiteratureReference:2060844] Achondroplasia is defined by recurrent G380R mutations of FGFR3
schemaClass	Person
surname	McIntosh

Cite Us!