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Association of interleukin-1 gene polymorphisms with sudden sensorineural hearing loss and Ménière’s disease

✍ Scribed by T. Furuta; M. Teranishi; Y. Uchida; N. Nishio; K. Kato; H. Otake; T. Yoshida; M. Tagaya; H. Suzuki; M. Sugiura; M. Sone; M. Hiramatsu; S. Sugiura; F. Ando; H. Shimokata; T. Nakashima

Book ID
114831754
Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
82 KB
Volume
38
Category
Article
ISSN
1744-3121

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✍ Yasue Uchida; Saiko Sugiura; Fujiko Ando; Hiroshi Shimokata; Tsutomu Nakashima 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 88 KB

## Abstract ## Objectives/Hypothesis: To investigate the recently reported association of the C677T polymorphism in the methylenetetrahydrofolate reductase (MTHFR) gene with sudden sensorineural hearing loss (SSNHL), we analyzed data from a community‐based Japanese population. ## Study Design: N