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Three families with ‘de novo’ m.3243A > G mutation
The m.3243A > G mutation is the most prevalent, disease-causing mitochondrial DNA (mtDNA) mutation. In a national cohort study of 48 families harbouring the m.3243A > G mutation, we identified three families in which the mutation appeared to occur sporadically within these families. In this re...
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| Опубликовано в: : | BBA Clin |
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| Главные авторы: | , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Elsevier
2016
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4900294/ https://ncbi.nlm.nih.gov/pubmed/27331024 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbacli.2016.04.007 |
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