Literature associating WFS1 and autosomal dominant nonsyndromic deafness 1
WFS1 [ENSP00000226760]
Wolfram syndrome 1 (wolframin); Participates in the regulation of cellular Ca(2+) homeostasis, at least partly, by modulating the filling state of the endoplasmic reticulum Ca(2+) store; Deafness associated genes
Synonyms: WFS1, WFS1p, hWFS1, B4DJ99, O76024 ...