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29. Human TRMU encoding the mitochondrial 5-methylaminomethyl-2-thiouridylate-methyltransferase is a putative nuclear modifier gene for the phenotypic expression of the deafness-associated 12S rRNA mutations. Yan Q, Bykhovskaya Y, Li R, Mengesha E, Shohat M, Estivill X, Fischel-Ghodsian N, Guan MX. Biochem Biophys Res Commun; 2006 Apr 21; 342(4):1130-6. PubMed ID: 16513084 [Abstract] [Full Text] [Related]
30. Deaf children identified through newborn hearing screening: parents' experiences of the diagnostic process. Tattersall H, Young A. Child Care Health Dev; 2006 Jan 21; 32(1):33-45. PubMed ID: 16398789 [Abstract] [Full Text] [Related]
31. [Prevention of deafness]. EWERTSEN HW. Nord Med; 1957 Jan 31; 57(5):161-5. PubMed ID: 13419110 [No Abstract] [Full Text] [Related]