Vona et al., 2021
- A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans.
Human genetics
140(6):915-931
Full text @ Hum. Genet.
Marker Type | Symbol | Name |
---|---|---|
Gene | clrn2 | clarin 2 |
Gene | pvalb9 | parvalbumin 9 |