Mitochondrial mutations in maternally inherited hearing loss-Reference-Cited by-同舟云学术

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Mitochondrial mutations in maternally inherited hearing loss

Published:2017-03-20 Issue:1 Volume:18 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Mutai Hideki,Watabe Takahisa,Kosaki Kenjiro,Ogawa Kaoru,Matsunaga Tatsuo

Funder

Grant-in-Aid for Clinical Research from National Hospital Organization of Japan

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/s12881-017-0389-4.pdf

Reference29 articles.

1. Kral A, O’Donoghue GM. Profound deafness in childhood. N Engl J Med. 2010;363:1438–50.

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

3. Anderson S, Bankier AT, Barrell BG, de Bruijn MH, Coulson AR, Drouin J, et al. Sequence and organization of the human mitochondrial genome. Nature. 1981;290:457–65.

4. Kokotas H, Petersen MB, Willems PJ. Mitochondrial deafness. Clin Genet. 2007;71:379–91.

5. Shoffner JM, Lott MT, Lezza AM, Seibel P, Ballinger SW, Wallace DC. Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation. Cell. 1990;61:931–7.

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