Frequency and clinical features of hearing loss caused by STRC deletions-Reference-Cited by-同舟云学术

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Frequency and clinical features of hearing loss caused by STRC deletions

Published:2019-03-13 Issue:1 Volume:9 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Yokota Yoh,Moteki Hideaki,Nishio Shin-ya^ORCID,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,Usami Shin-ichi^ORCID

Funder

Grant-in-Aid for Scientific Research (C) from the Ministry of Education, Science and Culture of Japan

Japan Agency for Medical Research and Development

Grant-in-Aid for Scientific Research (A) from the Ministry of Education, Science and Culture of Japan

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/s41598-019-40586-7.pdf

Reference20 articles.

1. Morton, C. C. & Nance, W. E. Newborn hearing screening–a silent revolution. New England Journal of Medicine 354, 2151–2164 (2006).

2. Zhang, F., Gu, W., Hurles, M. E. & Lupski, J. R. Copy number variation in human health, disease, and evolution. Annual Review of Genomics and Human Genetics 10, 451–481 (2009).

3. Conrad, D. F. et al. Origins and functional impact of copy number variation in the human genome. Nature 464, 704–712 (2010).

4. Shearer, A. E. et al. Copy number variants are a common cause of non-syndromic hearing loss. Genome Medicine 6, 37 (2014).

5. Francey, L. J. et al. Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment. American Journal of Medical Genetics part A. 158A, 298–308 (2012).

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