Multiple Consequences of a Single Amino Acid Pathogenic RTK Mutation: The A391E Mutation in FGFR3
Fenghao Chen(Johns Hopkins University), Kalina Hristova(Johns Hopkins University)
Cited by 12
Related Papers
Mechanism of FGF receptor dimerization and activation
|Nature Communications|2016|257
FGFR3 Heterodimerization in Achondroplasia, the Most Common Form of Human Dwarfism
|Journal of Biological Chemistry|2011|42
Consequences of replacing EGFR juxtamembrane domain with an unstructured sequence
|Scientific Reports|2012|32