COX deficiency and leukoencephalopathy due to a novel...

Neurology: Genetics 2020 / 08 Vol. 6; Iss. 4

COX deficiency and leukoencephalopathy due to a novel homozygous APOPT1/COA8 mutation

Hedberg-Oldfors, Carola, Darin, Niklas, Thomsen, Christer, Lindberg, Christopher, Oldfors, Anders
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Volume:
6
Journal:
Neurology Genetics
DOI:
10.1212/nxg.0000000000000464
Date:
August, 2020
File:
PDF, 747 KB
2020
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