Frequency and clinical features of hearing loss caused by STRC deletions
Frequency and clinical features of hearing loss caused by STRC deletions
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Author / Creator
Yokota, Yoh , Moteki, Hideaki , Nishio, Shin-ya , Yamaguchi, Tomomi , Wakui, Keiko , Kobayashi, Yumiko , Ohyama, Kenji , Miyazaki, Hiromitsu , Matsuoka, Rina , Abe, Satoko , Kumakawa, Kozo , Takahashi, Masahiro , Sakaguchi, Hirofumi , Uehara, Natsumi , Ishino, Takashi , Kosho, Tomoki , Fukushima, Yoshimitsu and Usami, Shin-ichi
Publisher
London: Nature Publishing Group UK
Journal title
Language
English
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Publication information
Publisher
London: Nature Publishing Group UK
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More information
Scope and Contents
Contents
Sensorineural hearing loss is a common deficit and mainly occurs due to genetic factors. Recently, copy number variants (CNVs) in the
STRC
gene have also been recognized as a major cause of genetic hearing loss. We investigated the frequency of
STRC
deletions in the Japanese population and the characteristics of associated hearing loss....
Alternative Titles
Full title
Frequency and clinical features of hearing loss caused by STRC deletions
Authors, Artists and Contributors
Author / Creator
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Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6416315
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6416315
Other Identifiers
ISSN
2045-2322
E-ISSN
2045-2322
DOI
10.1038/s41598-019-40586-7
