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Diagnostic and therapeutic aspects of Leigh syndrome due to the variant m.10197G>A

With interest we read the article by Tolomeo et al. about three unrelated males aged 7y (patient 1), 5y (patient 2) and 4y (patient 3) respectively with Leigh syndrome due to the variant m.10197G > A in the ND3 gene [1]. We have the following comments and concerns.

from Journal of the Neurological Sciences https://ift.tt/2UglgGA
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