Schulte et al., 2014
- Targeted resequencing and systematic in vivo functional testing identifies rare variants in MEIS1 as significant contributors to restless legs syndrome.
American journal of human genetics
95:85-95
Full text @ Am. J. Hum. Genet.
Target | Reagent |
---|---|
map2k5 | MO1-map2k5 |
meis1a | MO1-meis1 |
MO2-meis1 | |
meis1b | MO1-meis1 |
MO2-meis1 |