A nonsynonymous mutation in the WFS1 gene in a Finnish family with age-related hearing impairment
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DOI: 10.1016/j.heares.2017.09.013
Abstract: Abstract Wolfram syndrome (WS) is caused by recessive mutations in the Wolfram syndrome 1 (WFS1) gene. Sensorineural hearing impairment (HI) is a frequent feature in WS and, furthermore, certain mutations in WFS1 cause nonsyndromic dominantly… read more here.
Keywords: hearing impairment; wfs1; mutation wfs1; wfs1 gene ... See more keywords