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5. Novel IBA57 mutations in two chinese patients and literature review of multiple mitochondrial dysfunction syndrome. Zhan F; Liu X; Ni R; Liu T; Cao Y; Wu J; Tian W; Luan X; Cao L Metab Brain Dis; 2022 Feb; 37(2):311-317. PubMed ID: 34709542 [TBL] [Abstract][Full Text] [Related]
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11. Expanding the phenotype of IBA57 mutations: related leukodystrophy can remain asymptomatic. Hamanaka K; Miyatake S; Zerem A; Lev D; Blumkin L; Yokochi K; Fujita A; Imagawa E; Iwama K; Nakashima M; Mitsuhashi S; Mizuguchi T; Takata A; Miyake N; Saitsu H; van der Knaap MS; Lerman-Sagie T; Matsumoto N J Hum Genet; 2018 Dec; 63(12):1223-1229. PubMed ID: 30258207 [TBL] [Abstract][Full Text] [Related]
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