A Novel Mutation in the WFS1 gene in a Chinese Family with Autosomal Dominant Non-syndromic Hearing Loss
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ABSTRACT: Mutations in the WFS1 gene can cause Wolfram syndrome or autosomal dominant non-syndromic low-frequency hearing loss (HL). This study investigated the molecular basis of HL in an affected Chinese family.
TISSUE(S): Blood
SUBMITTER: Hongen,XU
PROVIDER: OEX009938 | NODE |
REPOSITORIES: NODE
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