Frequency of mitochondrial m.1555A > G mutation in Syrian patients with non-syndromic hearing impairment-Reference-Cited by-同舟云学术

Frequency of mitochondrial m.1555A > G mutation in Syrian patients with non-syndromic hearing impairment

Published:2018-05-21 Issue:1 Volume:18 Page:
ISSN:1472-6815
Container-title:BMC Ear, Nose and Throat Disorders
language:en
Short-container-title:BMC Ear Nose Throat Disord

Author:

Kaheel Hazem,Breß Andreas,Hassan Mohamed A.,Shah Aftab Ali,Amin Mutaz,Bakhit Yousuf H. Y.,Kniper Marlies

Publisher

Springer Science and Business Media LLC

Subject

Otorhinolaryngology

Link

http://link.springer.com/content/pdf/10.1186/s12901-018-0055-2.pdf

Reference20 articles.

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3. Schrijver I. Hereditary non-syndromic sensorineural hearing loss: transforming silence to sound. J Mol Diagn [Internet]. 2004 Nov [cited 2017 Apr 16];6(4):275–84. Available from: http://www.ncbi.nlm.nih.gov/pubmed/15507665 .

4. Smith RJ, Jones M-KN. Nonsyndromic Hearing Loss and Deafness, DFNB1 [Internet]. GeneReviews(®). University of Washington, Seattle; 1993 [cited 2017 Apr 18]. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20301449

5. Othman H, Saadat M. Prevalence of consanguineous marriages in syria. J Biosoc Sci [Internet]. 2009 Sep 12 [cited 2017 Apr 18];41(5):685. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19433003

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