Impact of Methionine Synthase Gene and Methylenetetrahydrofolate Reductase Gene Polymorphisms on the Risk of Sudden Sensorineural Hearing Loss - Gross, Menachem; Friedman, Gideon; Eliashar, Ron; Koren-Morag, Nira; Goldschmidt, Neta; Atta, Iman Abou; Ben-Yehuda, Arie (Audiology & neurotology, 2006)
Keywords: 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase - genetics; Adult; Aged; Biological and medical sciences; Case-Control Studies; Cochlea - blood supply; Ear, auditive nerve, cochleovestibular tract, facial nerve: diseases, semeiology; Female; Gene Frequency; Genotype; Hearing Loss, Sensorineural - etiology; Hearing Loss, Sensorineural - genetics; Hearing Loss, Sudden - etiology; Hearing Loss, Sudden - genetics; Humans; Male; Medical sciences; Methylenetetrahydrofolate Reductase (NADPH2) - genetics; Middle Aged; Non tumoral diseases; Original Paper; Otorhinolaryngology. Stomatology; Polymorphism, Genetic; Prospective Studies; Regression Analysis; Risk Factors; Vascular Diseases - complications; Vascular Diseases - genetics; Methylenetetrahydrofolate reductase; Methionine synthase; Sudden sensorineural hearing loss; Vascular impairment; O-Acetylhomoserine (thiol)-lyase; Enzyme; Internal ear disease; Auditory disorder; Risk; Lyases; Gene; Blood vessel; Sudden hearing loss; Risk factor; ENT disease; Perception hearing loss; Oxidoreductases; Carbon-oxygen lyases; Sensory hearing loss; Polymorphism; Reductase