Mutations in the Wolfram Syndrome Type 1 Gene (WFS1) Define a Clinical Entity of Dominant Low-Frequency Sensorineural Hearing Loss
Archives of Otolaryngology–Head & Neck Surgery
doi 10.1001/archotol.129.4.411
Full Text
Open PDFAbstract
Available in full text
Date
April 1, 2003
Authors
Publisher
American Medical Association (AMA)