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1-4 of 4 results for DFNB77

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Restricted accessResearch articleFirst published December, 2010

Mutations in TMC1 are a Common Cause of DFNB7/11 Hearing Loss in the Iranian Population

Michael S. Hildebrand, Kimia Kahrizi, Catherine J. Bromhead [...]

Annals of Otology,Rhinology & Laryngology

Restricted accessResearch articleFirst published May, 2015

Mutations in LOXHD1 Gene Cause Various Types and Severities of Hearing Loss

Kentaro Mori, Hideaki Moteki, Yumiko Kobayashi [...]

Annals of Otology,Rhinology & Laryngology

Open accessResearch articleFirst published December, 2019

A novel LOXHD1 variant in a Chinese couple with hearing loss

Chuan Zhang, Shengju Hao, Yali Liu [...]

Journal of International Medical Research

Restricted accessResearch articleFirst published May, 2012

The Common TMC1 Mutation c.100C>T (p.Arg34X) Is Not a Significant Cause of Deafness in British Asians

Claire Searle, Lampros A. Mavrogiannis, Christopher P. Bennett [...]

Genetic Testing and Molecular Biomarkers

Search results

Articles (4)

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1-4 of 4 results for DFNB77

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Restricted accessResearch articleFirst published December, 2010

Mutations in TMC1 are a Common Cause of DFNB7/11 Hearing Loss in the Iranian Population

Michael S. Hildebrand, Kimia Kahrizi, Catherine J. Bromhead [...]

Annals of Otology,Rhinology & Laryngology

Restricted accessResearch articleFirst published May, 2015

Mutations in LOXHD1 Gene Cause Various Types and Severities of Hearing Loss

Kentaro Mori, Hideaki Moteki, Yumiko Kobayashi [...]

Annals of Otology,Rhinology & Laryngology

Open accessResearch articleFirst published December, 2019

A novel LOXHD1 variant in a Chinese couple with hearing loss

Chuan Zhang, Shengju Hao, Yali Liu [...]

Journal of International Medical Research

Restricted accessResearch articleFirst published May, 2012

The Common TMC1 Mutation c.100C>T (p.Arg34X) Is Not a Significant Cause of Deafness in British Asians

Claire Searle, Lampros A. Mavrogiannis, Christopher P. Bennett [...]

Genetic Testing and Molecular Biomarkers