SOD1gene polymorphisms in sudden sensorineural hearing loss-Reference-Cited by-同舟云学术

SOD1gene polymorphisms in sudden sensorineural hearing loss

Published:2016-02-16 Issue:5 Volume:136 Page:465-469
ISSN:0001-6489
Container-title:Acta Oto-Laryngologica
language:en
Short-container-title:Acta Oto-Laryngologica

Author:

Kitoh Ryosuke,Nishio Shin-Ya,Ogawa Kaoru,Okamoto Makito,Kitamura Ken,Gyo Kiyofumi,Sato Hiroaki,Nakashima Tsutomu,Fukuda Satoshi,Fukushima Kunihiro,Hara Akira,Yamasoba Tatsuya,Usami Shin-ichi

Publisher

Informa UK Limited

Subject

Otorhinolaryngology,General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.3109/00016489.2015.1116047

Reference20 articles.

1. Genetic and Acquired Prothrombotic Risk Factors and Sudden Hearing Loss

2. Association of the C677T polymorphism in the methylenetetrahydrofolate reductase gene with sudden sensorineural hearing loss

3. Contribution of 1425G/A Polymorphism in Protein Kinase C-Eta (PRKCH) Gene and Brain White Matter Lesions to the Risk of Sudden Sensorineural Hearing Loss in a Japanese Nested Case-Control Study

4. Contribution of complement factor H Y402H polymorphism to sudden sensorineural hearing loss risk and possible interaction with diabetes

5. Candidate Genes of Cerebrovascular Disease and Sudden Sensorineural Hearing Loss

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