Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing-impaired subjects-Reference-Cited by-同舟云学术

Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing-impaired subjects

Published:2018-05-08 Issue:1 Volume:19 Page:
ISSN:1471-2350
Container-title:BMC Medical Genetics
language:en
Short-container-title:BMC Med Genet

Author:

Nonose Renata Watanabe,Lezirovitz Karina,de Mello Auricchio Maria Teresa Balester,Batissoco Ana Carla,Yamamoto Guilherme Lopes,Mingroni-Netto Regina Célia

Funder

FAPESP

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1186/s12881-018-0585-x.pdf

Reference52 articles.

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2. Smith RJH and Jones MN. Nonsyndromic Hearing Loss and Deafness, DFNB1 GeneReviews - NCBI Bookshelf. U.S. National Library of Medicine. 2017. http://www.ncbi.nlm.nih.gov/books/NBK1272/ . Accessed 15 Apr 2017.

3. Van Camp G and Smith RJH. Hereditary hearing loss homepage. 2017. http://hereditaryhearingloss.org . Accessed 31 Jan 2017.

4. Everett LA, Glaser B, Beck JC, Idol JR, Buchs A, Heyman M, Adawi F, Hazani E, Nassir E, Baxevanis AD, Sheffield VC, Green ED. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS). Nature Genet. 1997;17:411–22.

5. Alasti F, Van Camp G, and Smith RJH. Pendred Syndrome/DFNB4” GeneReviews - NCBI Bookshelf. U.S National Library of Medicine 2017. http://www.ncbi.nlm.nih.gov/books/NBK1467 /. Accessed 20 Apr 2017.

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