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A mitochondrial DNA D loop insertion detected almost exclusively in non-replicating tissues with maternal inheritance across three generations.
Sharma, Mehul A; Lee, Ja Young J; Tam, Andrea; Sattha, Beheroze; Mackenzie, Ian R; Vallance, Hilary D; Sirrs, Sandra; Hannah-Shmouni, Fady; Côté, Hélène C F; Mattman, Andre.
Afiliação
  • Sharma MA; Department of Pathology and Laboratory Medicine, The University of British Columbia, Canada.
  • Lee JYJ; Department of Pathology and Laboratory Medicine, The University of British Columbia, Canada.
  • Tam A; Department of Pathology and Laboratory Medicine, The University of British Columbia, Canada.
  • Sattha B; Department of Pathology and Laboratory Medicine, The University of British Columbia, Canada.
  • Mackenzie IR; Department of Pathology and Laboratory Medicine, The University of British Columbia, Canada; Division of Neuropathology, Department of Pathology and Laboratory Medicine, Vancouver General Hospital, The University of British Columbia, Canada.
  • Vallance HD; Department of Pathology and Laboratory Medicine, The University of British Columbia, Canada; Biochemical Genetics, Department of Pathology and Laboratory Medicine, Children's & Women's Health Centre of BC, The University of British Columbia, Canada.
  • Sirrs S; Adult Metabolic Diseases Clinic, Vancouver General Hospital, The University of British Columbia, Canada.
  • Hannah-Shmouni F; Adult Metabolic Diseases Clinic, Vancouver General Hospital, The University of British Columbia, Canada.
  • Côté HCF; Department of Pathology and Laboratory Medicine, The University of British Columbia, Canada.
  • Mattman A; Department of Pathology and Laboratory Medicine, The University of British Columbia, Canada; Adult Metabolic Diseases Clinic, Vancouver General Hospital, The University of British Columbia, Canada. Electronic address: amattman@providencehealth.bc.ca.
Mitochondrion ; 46: 298-301, 2019 05.
Article em En | MEDLINE | ID: mdl-30114489
Muscle biopsy identified a possibly pathogenic, mitochondrial DNA D-loop insertion, in each of 5 family members from two generations, that was otherwise undetectable in most other tissues. The tissue specific regulation of heteroplasmy is reflected in an age related increase in muscle heteroplasmy level, across the pedigree. This latter finding is in keeping with previous reports (e.g. T408A, C16327) but differs in having a very high muscle heteroplasmy level, and appears maternally transmitted.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Mutagênese Insercional / Músculo Esquelético / Doenças Mitocondriais / Herança Materna Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: DNA Mitocondrial / Mutagênese Insercional / Músculo Esquelético / Doenças Mitocondriais / Herança Materna Idioma: En Ano de publicação: 2019 Tipo de documento: Article