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.
Target | Reagent |
---|---|
fgfr1a | MO1-fgfr1a |
fgfr1b | MO1-fgfr1b |