Excess of Rare Missense Variants in Hearing Loss Genes in Sporadic Meniere Disease-Reference-Cited by-同舟云学术

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Excess of Rare Missense Variants in Hearing Loss Genes in Sporadic Meniere Disease

Published:2019-02-15 Issue: Volume:10 Page:
ISSN:1664-8021
Container-title:Frontiers in Genetics
language:
Short-container-title:Front. Genet.

Author:

Gallego-Martinez Alvaro,Requena Teresa,Roman-Naranjo Pablo,Lopez-Escamez Jose A.

Funder

Consejería de Salud, Junta de Andalucía

Publisher

Frontiers Media SA

Subject

Genetics(clinical),Genetics,Molecular Medicine

Reference45 articles.

1. Screening of the USH1G gene among Spanish Patients with Usher Syndrome. Lack of mutations and evidence of a minor role in the pathogenesis of the syndrome;Aller;Ophthalm. Genet.,2007

2. Genetic aspects of Familial Ménière's disease;Arweiler-Harbeck;Otol. Neurotol.,2011

3. The common variants/multiple disease hypothesis of common complex genetic disorders;Becker;Med. Hypotheses,2004

4. Pathogenetic role of the deafness-related M34T mutation of Cx26;Bicego;Hum. Mol. Genet.,2006

5. Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle Eastern Families;Brownstein;Genome Biol.,2011

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