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.
| Marker Type | Symbol | Name |
|---|---|---|
| Gene | sec61a1a | SEC61 translocon subunit alpha 1a |
| Gene | sec61a1b | SEC61 translocon subunit alpha 1b |