POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss-Reference-Cited by-同舟云学术

POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss

Published:2017-05-17 Issue:5 Volume:12 Page:e0177636
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Kitano Tomohiro,Miyagawa Maiko,Nishio Shin-ya,Moteki Hideaki,Oda Kiyoshi,Ohyama Kenji,Miyazaki Hiromitsu,Hidaka Hiroshi,Nakamura Ken-ichi,Murata Takaaki,Matsuoka Rina,Ohta Yoko,Nishiyama Nobuhiro,Kumakawa Kozo,Furutate Sakiko,Iwasaki Satoshi,Yamada Takechiyo,Ohta Yumi,Uehara Natsumi,Noguchi Yoshihiro,Usami Shin-ichi^ORCID

Funder

Japan Agency for Medical Research and Development

Ministry of Health, Labour and Welfare

Ministry of Education, Culture, Sports, Science, and Technology

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference44 articles.

1. Function and expression pattern of nonsyndromic deafness genes;N Hilgert;Curr Mol Med,2009

2. Van Camp G, Smith R. The Hereditary Hearing Loss homepage. http://hereditaryhearingloss.org/. Accessed September 20, 2016.

3. Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans;O Vahava;Science,1998