화학공학소재연구정보센터
검색결과 : 2건
No. Article
1 Study of modifiers factors associated to mitochondrial mutations in individuals with hearing impairment
de Moraes VCS, Alexandrino F, Andrade PB, Camara MF, Sartorato EL
Biochemical and Biophysical Research Communications, 381(2), 210, 2009
2 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 QF, Bykhovskaya Y, Li RH, Mengesha E, Shohat M, Estivill X, Fischel-Ghodsian N, Guan MX
Biochemical and Biophysical Research Communications, 342(4), 1130, 2006