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PDF Availablehttps://doi.org/10.1136/jmedgenet-2017-104891
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Cite Journal: Journal of Medical Genetics |  Publication Date: Nov 3, 2017 |
 Citations: 60 |
Affiliation: Drottning Silvias barn- och ungdomssjukhus, University of Bergen, Haukeland University Hospital, University of Helsinki, Helsinki University Hospital, Karolinska University Hospital, Copenhagen University Hospital, Rigshospitalet, University of Gothenburg, Oulu University Hospital, University of Oulu
BackgroundLeigh syndrome is a phenotypically and genetically heterogeneous mitochondrial disorder. While some genetic defects are associated with well-described phenotypes, phenotype-genotype correlations in Leigh syndrome are not fully explored.ObjectiveWe aimed to...
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