Genetic heterogeneity of mitochondrial genome in thiamine deficient Leigh syndrome patients
Author:
Funder
Council of Scientific and Industrial Research, India
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference70 articles.
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2. Biparental inheritance of mitochondrial DNA in humans;Luo;Proc. Natl. Acad. Sci. U. S. A.,2018
3. Heteroplasmic mtDNA mutation (T----G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high;Tatuch;Am. J. Hum. Genet.,1992
4. Nuclear DNA origin of cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence based on patient's-derived rho° transformants;Tiranti;Hum. Mol. Genet.,1995
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