Hong et al., 2016 - Dominant-negative Kinase Domain Mutations in FGFR1 Can Explain the Clinical Severity of Hartsfield Syndrome. Human molecular genetics   25(10):1912-1922 Full text @ Hum. Mol. Genet.
Morpholino List (2 Records)
Target Reagent
fgfr1a MO1-fgfr1a
fgfr1b MO1-fgfr1b