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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 7, 2024. (Total: 234175Documents)
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Records 1 - 2 (of 2 Records)

Query Trace: Hearing Loss and PRKCH[original query]
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.
Journal of neurogenetics 2011 Oct 25 (3): 82-7.
Uchida Yasue, Sugiura Saiko, Nakashima Tsutomu, Ando Fujiko, Shimokata Hiros
SOD1 gene polymorphisms in sudden sensorineural hearing loss.
Acta oto-laryngologica 2016 Feb 1-5.
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-Ic
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