Molecular basis of Leigh syndrome: a current look | Orphanet Journal of Rare Diseases | Full Text

Molecular basis of Leigh syndrome: a current look | Orphanet Journal of Rare Diseases | Full Text

Molecular basis of Leigh syndrome: a current look

Leigh Syndrome (OMIM 256000) is a heterogeneous neurologic disorder due to damage in mitochondrial energy production that usually starts in early childhood. The first description given by Leigh pointed out neu...

Authors:Manuela Baldo Schubert and Laura Vilarinho

Citation:Orphanet Journal of Rare Diseases 2020 15:31

Content type:Review

Published on: 29 January 2020

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