Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies

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dc.contributor.author Filosto, M.
dc.contributor.author Mancuso, M.
dc.contributor.author Vives-Bauza, C.
dc.contributor.author Vilà, M.R.
dc.contributor.author Shanske, S.
dc.contributor.author Hirano, M.
dc.contributor.author Andreu, AL.
dc.contributor.author DiMauro, S.
dc.date.accessioned 2020-05-06T08:16:50Z
dc.identifier.uri http://hdl.handle.net/11201/152248
dc.description.abstract [eng] In 2002, paternal inheritance of muscle mitochondrial DNA (mtDNA) was reported in a patient with exercise intolerance and a mitochondrial DNA (mtDNA) mutation restricted to skeletal muscle. To evaluate whether paternal inheritance is a common phenomenon, we studied 10 sporadic patients with skeletal muscle-restricted mtDNA mutations: five harbored mtDNA point mutations in protein-coding genes and five had single mtDNA deletions. We performed haplotype analysis and direct sequencing of the hypervariable regions 1 and 2 of the D-loop in muscle and blood from the patients and, when available, in blood from their parents. We did not observe paternal inheritance in any of our patients.
dc.format application/pdf
dc.relation.isformatof https://doi.org/10.1002/ana.10709
dc.relation.ispartof Annals of Neurology, 2003, vol. 54, num. 4, p. 524-526
dc.rights , 2003
dc.subject.classification 57 - Biologia
dc.subject.other 57 - Biological sciences in general
dc.title Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies
dc.type info:eu-repo/semantics/article
dc.date.updated 2020-05-06T08:16:50Z
dc.date.embargoEndDate info:eu-repo/date/embargoEnd/2026-12-31
dc.embargo 2026-12-31
dc.rights.accessRights info:eu-repo/semantics/embargoedAccess
dc.identifier.doi https://doi.org/10.1002/ana.10709


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