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 journalArticlepeer-review

65 Scopus citations

Fingerprint

Dive into the research topics of 'Mitochondrial myopathy, sideroblastic anemia, and lactic acidosis: An automosal recessive syndrome in persian jews caused by a mutation in the PUS1 gene'. Together they form a unique fingerprint.

Medicine & Life Sciences