Found: 1
Select item for more details and to access through your institution.
Novel loss-of-function mutations in COCH cause autosomal recessive nonsyndromic hearing loss.
- Published in:
- Human Genetics, 2020, v. 139, n. 12, p. 1565, doi. 10.1007/s00439-020-02197-5
- By:
- Publication type:
- Article