OTOF mutation analysis with massively parallel DNA sequencing in 2,265 Japanese sensorineural hearin...
OTOF mutation analysis with massively parallel DNA sequencing in 2,265 Japanese sensorineural hearing loss patients
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Author / Creator
Iwasa, Yoh-ichiro , Nishio, Shin-ya , Sugaya, Akiko , Kataoka, Yuko , Kanda, Yukihiko , Taniguchi, Mirei , Nagai, Kyoko , Naito, Yasushi , Ikezono, Tetsuo , Horie, Rie , Sakurai, Yuika , Matsuoka, Rina , Takeda, Hidehiko , Abe, Satoko , Kihara, Chiharu , Ishino, Takashi , Morita, Shin-ya , Iwasaki, Satoshi , Takahashi, Masahiro , Ito, Tsukasa , Arai, Yasuhiro and Usami, Shin-ichi
Publisher
United States: Public Library of Science
Journal title
Language
English
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Publication information
Publisher
United States: Public Library of Science
Subjects
More information
Scope and Contents
Contents
The OTOF gene (Locus: DFNB9), encoding otoferlin, is reported to be one of the major causes of non-syndromic recessive sensorineural hearing loss, and is also reported to be the most common cause of non-syndromic recessive auditory neuropathy spectrum disorder (ANSD). In the present study, we performed OTOF mutation analysis using massively paralle...
Alternative Titles
Full title
OTOF mutation analysis with massively parallel DNA sequencing in 2,265 Japanese sensorineural hearing loss patients
Authors, Artists and Contributors
Author / Creator
Nishio, Shin-ya
Sugaya, Akiko
Kataoka, Yuko
Kanda, Yukihiko
Taniguchi, Mirei
Nagai, Kyoko
Naito, Yasushi
Ikezono, Tetsuo
Horie, Rie
Sakurai, Yuika
Matsuoka, Rina
Takeda, Hidehiko
Abe, Satoko
Kihara, Chiharu
Ishino, Takashi
Morita, Shin-ya
Iwasaki, Satoshi
Takahashi, Masahiro
Ito, Tsukasa
Arai, Yasuhiro
Usami, Shin-ichi
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_plos_journals_2226434275
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_2226434275
Other Identifiers
ISSN
1932-6203
E-ISSN
1932-6203
DOI
10.1371/journal.pone.0215932
