Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss (Q28205421)
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scientific article (publication date: 15 October 2001)
Language | Label | Description | Also known as |
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English | Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss |
scientific article (publication date: 15 October 2001) |
Statements
Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss (English)
I N Bespalova
S J Bom
D J Brown
K Cryns
A T DeWan
K Flothmann
H P Kunst
P Kurnool
T A Sivakumaran
C W Cremers
S M Leal
M Burmeister
15 October 2001
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