Mitochondrial Myopathy, Sideroblastic Anemia, and Lactic Acidosis: An Autosomal Recessive Syndrome in Persian Jews Caused by a Mutation in the PUS1 Gene
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D. Lev | Y. Bykhovskaya | T. Lerman-Sagie | K. Casas | N. Fischel‐Ghodsian | M. Mimouni | A. Zeharia | Hana Tamari