Genetics of mitochondrial diseases: Identifying mutations to help diagnosis
Author:
Funder
BMBF
Publisher
Elsevier BV
Subject
General Biochemistry, Genetics and Molecular Biology,General Medicine
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4. Repetitive brainstem lesions in mitochondrial DNA 11778G>A mutation of Leber hereditary optic neuropathy;Miyaue;eNeurologicalSci.,2019
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