Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Hearing and CFH[original query] |
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The dot-and-fleck retinopathy of X linked Alport syndrome is independent of complement factor H (CFH) gene polymorphisms. The British journal of ophthalmology 2009 Mar 93 (3): 379-82. Liu J, Colville D, Wang Y Y, Baird P N, Guymer R H, Savige |
Contribution of complement factor H Y402H polymorphism to sudden sensorineural hearing loss risk and possible interaction with diabetes. Gene 2012 May 499 (1): 226-30. Nishio Naoki, Teranishi Masaaki, Uchida Yasue, Sugiura Saiko, Ando Fujiko, Shimokata Hiroshi, Sone Michihiko, Otake Hironao, Kato Ken, Yoshida Tadao, Tagaya Mitsuhiko, Hibi Tatsuya, Nakashima Tsuto |
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- Page last updated:Apr 22, 2024
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