Bolar et al., 2016
- Heterozygous Loss-of-Function SEC61A1 Mutations Cause Autosomal-Dominant Tubulo-Interstitial and Glomerulocystic Kidney Disease with Anemia.
American journal of human genetics
99:174-187
Full text @ Am. J. Hum. Genet.
Target | Reagent |
---|---|
sec61a1b | CRISPR1-sec61a1b |
CRISPR2-sec61a1b |