Human Genome Epidemiology Literature Finder
|
Records 1 - 3 (of 3 Records) |
| Query Trace: Hearing and NOS3[original query] |
|---|
| Polymorphisms in genes involved in the free-radical process in patients with sudden sensorineural hearing loss and Ménière's disease. Free radical research 2013 Jul 47 (6-7): 498-506. Teranishi M, Uchida Y, Nishio N, Kato K, Otake H, Yoshida T, Suzuki H, Sone M, Sugiura S, Ando F, Shimokata H, Nakashima |
| Prognostic impact of gene polymorphisms in patients with idiopathic sudden sensorineural hearing loss. Acta oto-laryngologica 2017 Apr 1-6. Kitoh Ryosuke, Nishio Shin-Ya, Usami Shin-Ic |
| Rare Variants of Putative Candidate Genes Associated With Sporadic Meniere's Disease in East Asian Population. Frontiers in neurology 2019 10 1424. Oh Eun Hye, Shin Jin-Hong, Kim Hyang-Sook, Cho Jae Wook, Choi Seo Young, Choi Kwang-Dong, Rhee Je-Keun, Lee Seowhang, Lee Changwook, Choi Jae-Hw |
- Page last reviewed:Feb 1, 2024
- Content source:

