Is PNPT1-related hearing loss ever non-syndromic? Whole exome sequencing of adult siblings expands the natural history of PNPT1-related disorders. [electronic resource]

By: Contributor(s): Producer: 20190925Description: 2487-2493 p. digitalISSN:
  • 1552-4833
Subject(s): Online resources: In: American journal of medical genetics. Part A vol. 176
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

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