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.
CRISPR List (2 Records)
Target Reagent
sec61a1l CRISPR1-sec61a1l
CRISPR2-sec61a1l