Mitochondrial myopathy, sideroblastic anemia, and lactic acidosis: An automosal recessive syndrome in persian jews caused by a mutation in the PUS1 gene

Avraham Zeharia, Nathan Fischel-Ghodsian, Kari Casas, Yelena Bykhovskaya, Hana Tamari, Dorit Lev, Marc Mimouni, Tally Lerman-Sagie*

*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

66 Scopus citations

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Medicine and Dentistry

Biochemistry, Genetics and Molecular Biology