MARVELD2 (DFNB49) Mutations in the Hearing Impaired Central European Roma Population - Prevalence, Clinical Impact and the Common Origin-Reference-Cited by-同舟云学术

MARVELD2 (DFNB49) Mutations in the Hearing Impaired Central European Roma Population - Prevalence, Clinical Impact and the Common Origin

Published:2015-04-17 Issue:4 Volume:10 Page:e0124232
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Mašindová Ivica,Šoltýsová Andrea,Varga Lukáš,Mátyás Petra,Ficek Andrej,Hučková Miloslava,Sůrová Martina,Šafka-Brožková Dana,Anwar Saima,Bene Judit,Straka Slavomír,Janicsek Ingrid,Ahmed Zubair M.,Seeman Pavel,Melegh Béla,Profant Milan,Klimeš Iwar,Riazuddin Saima,Kádasi Ľudevít,Gašperíková Daniela

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference39 articles.

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2. Van Camp G, Smith RJ. Hereditary hearing loss homepage. Accessed 10 Sept 2014. Available: http://hereditaryhearingloss.org/

3. A new locus for nonsyndromic deafness DFNB49 maps to chromosome 5q12.3-q14.1;K Ramzan;Hum Genet,2005

4. Tricellulin is a tight-junction protein necessary for hearing;S Riazuddin;Am J Hum Genet,2006

5. Tricellulin constitutes a novel barrier at tricellular contacts of epithelial cells;J Ikenouchi;J Cell Biol,2005

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