Screening of the SLC17A8 gene as a causative factor for autosomal dominant non-syndromic hearing loss in Koreans-Reference-Cited by-同舟云学术

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Screening of the SLC17A8 gene as a causative factor for autosomal dominant non-syndromic hearing loss in Koreans

Published:2016-01-22 Issue:1 Volume:17 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Ryu Nari,Sagong Borum,Park Hong-Joon,Kim Min-A,Lee Kyu-Yup,Choi Jae Young,Kim Un-Kyung

Funder

Korea Health Industry Development Institute (KR)

National Research Foundation of Korea (KR)

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/s12881-016-0269-3

Reference23 articles.

1. Morton NE. Genetic epidemiology of hearing impairment. Ann N Y Acad Sci. 1991;630:16–31.

2. Morton CC, Nance WE. Newborn hearing screening--a silent revolution. N Engl J Med. 2006;354(20):2151–64.

3. Morton CC. Genetics, genomics and gene discovery in the auditory system. Hum Mol Genet. 2002;11(10):1229–40.

4. Smith RJ, Bale Jr JF, White KR. Sensorineural hearing loss in children. Lancet. 2005;365(9462):879–90.

5. Parker MA. Biotechnology in the treatment of sensorineural hearing loss: foundations and future of hair cell regeneration. J Speech Lang Hear Res. 2011;54(6):1709–31.

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