Deafness genetic mutation discovered

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Date: 2015-03-03 23:13:06 Mitochondrial diseases Channelopathy Genetic genealogy Nonsyndromic deafness Syndromes Usher syndrome Stereocilia Wolfram syndrome Usher 1C Genetics Deafness Health		Deafness genetic mutation discovered Add to Reading List Source URL: medicalxpress.com Download Document from Source Website File Size: 15,43 KB Share Document on Facebook

	Continuing Medical Education Credits (CMEs) The American College of Medical Genetics and Genomics (ACMG) has designated the ASHG 2018 Annual Meeting for a maximum of 31.5 AMA PRA Category 1 Credit(s). Physicians should c DocID: 1xVNt - View Document
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