Halbritter et al., 2013
- Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans.
American journal of human genetics
93(5):915-925
Full text @ Am. J. Hum. Genet.
Target | Reagent |
---|---|
ift80 | MO1-ift80 |
ift172 | MO2-ift172 |
MO3-ift172 |