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
sec61a1b CRISPR1-sec61a1b
CRISPR2-sec61a1b
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