Defective complex III mitochondrial respiratory chain due to a novel variant in CYC1 gene masquerades acute demyelinating syndrome or Leber hereditary optic neuropathy
Autor: | Heidari, Erfan, Rasoulinezhad, Maryam, Pak, Neda, Reza Ashrafi, Mahmoud, Heidari, Morteza, Banwell, Brenda, Garshasbi, Masoud, Reza Tavasoli, Ali |
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Zdroj: | In Mitochondrion September 2021 60:12-20 |
Databáze: | ScienceDirect |
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