v1
Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1.
Identifier:nobleid.org/w1/20260515/8F62DF07
Type:Journal Article
0 views
Embeddable Badge
[](https://nobleid.org/work/w1/20260515/8F62DF07)
Bibliometric Analysis
Impact metrics, research fronts, co-authorship networks →
Authors & Claims