Identification of two novel missense WFS1 mutations, H696Y and R703H, in patients with non-syndromic low-frequency sensorineural hearing loss

Title
Identification of two novel missense WFS1 mutations, H696Y and R703H, in patients with non-syndromic low-frequency sensorineural hearing loss
Authors
Keywords
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Journal
Journal of Genetics and Genomics
Volume 38, Issue 2, Pages 71-76
Publisher
Elsevier BV
Online
2011-02-09
DOI
10.1016/j.jcg.2011.01.001

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