<it>GJB2 </it>mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment
<p>Abstract</p> <p>Background</p> <p>Mutations in <it>GJB2 </it>are the most common molecular defects responsible for autosomal recessive nonsyndromic hearing impairment (NSHI). The mutation spectra of this gene vary among different ethnic groups.</p>...
Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2009-04-01
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Series: | Journal of Translational Medicine |
Online Access: | http://www.translational-medicine.com/content/7/1/26 |