A POU3F4 Mutation Causes Nonsyndromic Hearing Loss in a Chinese X-linked Recessive Family
Background: The molecular genetic research showed the association between X-linked hearing loss and mutations in POU3F4. This research aimed to identify a POU3F4 mutation in a nonsyndromic X-linked recessive hearing loss family. Methods: A series of clinical evaluations including medical history, ot...
| Main Authors: | , , , , , , , , , , , |
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| פורמט: | Article |
| שפה: | English |
| יצא לאור: |
Wolters Kluwer
2017-01-01
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| סדרה: | Chinese Medical Journal |
| נושאים: | |
| גישה מקוונת: | http://www.cmj.org/article.asp?issn=0366-6999;year=2017;volume=130;issue=1;spage=88;epage=92;aulast=Du |