Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss.

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Bespalova I., Van Camp G., Bom S., Brown D., Cryns K., DeWan A., ...More

AMERICAN JOURNAL OF HUMAN GENETICS, vol.69, no.4, pp.230, 2001 (SCI-Expanded)

• Publication Type: Article / Abstract
• Volume: 69 Issue: 4
• Publication Date: 2001
• Journal Name: AMERICAN JOURNAL OF HUMAN GENETICS
• Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
• Page Numbers: pp.230
• Middle East Technical University Affiliated: Yes