Loss-of-Function Mutations in the PRPS1 Gene Cause a Type of Nonsyndromic X-linked Sensorineural Deafness, DFN2

Published 2009 View Full Article

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Title
Loss-of-Function Mutations in the PRPS1 Gene Cause a Type of Nonsyndromic X-linked Sensorineural Deafness, DFN2
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF HUMAN GENETICS
Volume 86, Issue 1, Pages 65-71
Publisher
Elsevier BV
Online
2009-12-18
DOI
10.1016/j.ajhg.2009.11.015

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