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Clinical Genetics, ISSN 0009-9163, 04/2018, Volume 93, Issue 4, pp. 925 - 928
Carriers of the mitochondrial mutation m.3243A>G presents highly variable phenotypes including mitochondrial encephalomyopathy, lactoacidosis and stroke‐like... 
heteroplasmy | MELAS | m.3243A>G | mitochondria | DIAGNOSIS | MANAGEMENT | LEUKOCYTES | MITOCHONDRIAL-DNA HETEROPLASMY | GENETICS & HEREDITY | m.3243A > G | DEAFNESS | ENCEPHALOMYOPATHY | MTDNA MUTATION | BLOOD | Mortality | Genetic aspects | Mitochondria | Mutation | MELAS syndrome | Heteroplasmy
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 08/2013, Volume 84, Issue 8, pp. 936 - 938
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 02/2009, Volume 360, Issue 6, pp. 640 - 642
Journal Article
Journal Article
Oncogene, ISSN 0950-9232, 08/2006, Volume 25, Issue 34, pp. 4647 - 4662
Journal Article