Literature DB >> 12408061

DFNA2/KCNQ4 and its manifestations.

Els M R De Leenheer1, Robbert J H Ensink, Henricus P M Kunst, Henri A M Marres, Zohreh Talebizadeh, Frank Declau, Shelley D Smith, Shin-ichi Usami, Paul H Van de Heyning, Guy Van Camp, Patrick L M Huygen, Cor W R J Cremers.   

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Year:  2002        PMID： 12408061     DOI： 10.1159/000066802

Source DB:  PubMed          Journal:  Adv Otorhinolaryngol        ISSN： 0065-3071


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  7 in total

1.  Mice with altered KCNQ4 K+ channels implicate sensory outer hair cells in human progressive deafness.

Authors:  Tatjana Kharkovets; Karin Dedek; Hannes Maier; Michaela Schweizer; Darina Khimich; Régis Nouvian; Vitya Vardanyan; Rudolf Leuwer; Tobias Moser; Thomas J Jentsch
Journal:  EMBO J       Date:  2006-01-26       Impact factor: 11.598

Review 2.  KV7 channelopathies.

Authors:  Snezana Maljevic; Thomas V Wuttke; Guiscard Seebohm; Holger Lerche
Journal:  Pflugers Arch       Date:  2010-04-18       Impact factor: 3.657

3.  Developmental expression of Kcnq4 in vestibular neurons and neurosensory epithelia.

Authors:  Sonia M S Rocha-Sanchez; Kenneth A Morris; Bechara Kachar; David Nichols; Bernd Fritzsch; Kirk W Beisel
Journal:  Brain Res       Date:  2007-01-08       Impact factor: 3.252

4.  Application of a New Genetic Deafness Microarray for Detecting Mutations in the Deaf in China.

Authors:  Hong Wu; Yong Feng; Lu Jiang; Qian Pan; Yalan Liu; Chang Liu; Chufeng He; Hongsheng Chen; Xueming Liu; Chang Hu; Yiqiao Hu; Lingyun Mei
Journal:  PLoS One       Date:  2016-03-28       Impact factor: 3.240

5.  Audioprofile-directed screening identifies novel mutations in KCNQ4 causing hearing loss at the DFNA2 locus.

Authors:  Michael S Hildebrand; Dylan Tack; Sarah J McMordie; Adam DeLuca; In Ae Hur; Carla Nishimura; Patrick Huygen; Thomas L Casavant; Richard J H Smith
Journal:  Genet Med       Date:  2008-11       Impact factor: 8.822

6.  Genetics of hearing loss: focus on DFNA2.

Authors:  Laura M Dominguez; Kelley M Dodson
Journal:  Appl Clin Genet       Date:  2012-10-18

Review 7.  Molecular genetics of non-syndromic deafness.

Authors:  Vânia B Piatto; Ellen C T Nascimento; Fabiana Alexandrino; Camila A Oliveira; Ana Cláudia P Lopes; Edi Lúcia Sartorato; José Victor Maniglia
Journal:  Braz J Otorhinolaryngol       Date:  2005-08-02
  7 in total

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