dc.contributor.author |
Filosto, M.
|
|
dc.contributor.author |
Mancuso, M.
|
|
dc.contributor.author |
Vives-Bauza, C.
|
|
dc.contributor.author |
Vilà, M.R.
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|
dc.contributor.author |
Shanske, S.
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|
dc.contributor.author |
Hirano, M.
|
|
dc.contributor.author |
Andreu, AL.
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|
dc.contributor.author |
DiMauro, S.
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|
dc.date.accessioned |
2020-05-06T08:16:50Z |
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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. |
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dc.format |
application/pdf |
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dc.relation.isformatof |
https://doi.org/10.1002/ana.10709 |
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dc.relation.ispartof |
Annals of Neurology, 2003, vol. 54, num. 4, p. 524-526 |
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dc.rights |
, 2003 |
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dc.subject.classification |
57 - Biologia |
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dc.subject.other |
57 - Biological sciences in general |
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dc.title |
Lack of paternal inheritance of muscle mitochondrial DNA in sporadic mitochondrial myopathies |
|
dc.type |
info:eu-repo/semantics/article |
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dc.date.updated |
2020-05-06T08:16:50Z |
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dc.date.embargoEndDate |
info:eu-repo/date/embargoEnd/2026-12-31 |
|
dc.embargo |
2026-12-31 |
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dc.rights.accessRights |
info:eu-repo/semantics/embargoedAccess |
|
dc.identifier.doi |
https://doi.org/10.1002/ana.10709 |
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