Contribution of complement factor H Y402H polymorphism to sudden sensorineural hearing loss risk and possible interaction with diabetes - Nishio, Naoki; Teranishi, Masaaki; Uchida, Yasue; Sugiura, Saiko; Ando, Fujiko; Shimokata, Hiroshi; Sone, Michihiko; Otake, Hironao; Kato, Ken; Yoshida, Tadao; Tagaya, Mitsuhiko; Hibi, Tatsuya; et al. (Gene, 2012)
Keywords: Adult; Aged; Aged, 80 and over; alleles; Amino Acid Substitution; Amino Acid Substitution - genetics; Amino Acid Substitution - physiology; Case-Control Studies; CFH Y402H; complement; Complement Factor H; Complement Factor H - genetics; complications; confidence interval; Diabetes; Diabetes Complications; Diabetes Complications - genetics; etiology; Female; Gene-Environment Interaction; Genetic Predisposition to Disease; genetics; hearing; Hearing Loss, Sensorineural; Hearing Loss, Sensorineural - complications; Hearing Loss, Sensorineural - genetics; Hearing Loss, Sudden; Hearing Loss, Sudden - complications; Hearing Loss, Sudden - genetics; Histidine; Histidine - genetics; Humans; hyperlipidemia; hypertension; macular degeneration; Male; Middle Aged; odds ratio; patients; physiology; Polymorphism; Polymorphism, Single Nucleotide; Polymorphism, Single Nucleotide - physiology; risk; Sudden sensorineural hearing loss; Tyrosine; Tyrosine - genetics; Young Adult; CRP; OR; CFH; SAS; CFH Y402H; CI; aHUS; MPGN2; SSNHL; Sudden sensorineural hearing loss; Complement factor H; NILS-LSA; AMD; Diabetes; PCR; Polymorphism