Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia-Reference-Cited by-同舟云学术

Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia

Published:2018-08-07 Issue:1 Volume:19 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Zytsar Marina V.,Barashkov Nikolay A.,Bady-Khoo Marita S.,Shubina-Olejnik Olga A.,Danilenko Nina G.,Bondar Alexander A.,Morozov Igor V.,Solovyev Aisen V.,Danilchenko Valeriia Yu.,Maximov Vladimir N.,Posukh Olga L.^ORCID

Funder

Project of Institute of Cytology and Genetics SB RAS

Russian Foundation for Basic Research

Government Task of Ministry of Education and Science of the Russian Federation

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/s12881-018-0650-5.pdf

Reference54 articles.

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3. Liu XZ, Xia XJ, Ke XM, Ouyang XM, Du LL, Liu YH, Angeli S, Telischi FF, Nance WE, Balkany T, et al. The prevalence of connexin 26 (GJB2) mutations in the Chinese population. Hum Genet. 2002;111:394–7.

4. Ohtsuka A, Yuge I, Kimura S, Namba A, Abe S, Van Laer L, Van Camp G, Usami S. GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation. Hum Genet. 2003;112(4):329–33.

5. Morell RJ, Kim HJ, Hood LJ, Goforth L, Friderici K, Fisher R, Van Camp G, Berlin CI, Oddoux C, Ostrer H, et al. Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness. N Engl J Med. 1998;339:1500–5.

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