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.
2 Genes / Markers
Marker Type Symbol Name
Gene sec61a1 SEC61 translocon subunit alpha 1
Gene sec61a1l SEC61 translocon subunit alpha 1, like