CrossRef Text and Data Mining
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Screening for Mitochondrial DNA Mutations of MELAS tRNA Leu(3243), MERRF tRNA Lys(8344) in Korean IDDM Patients.
Han Wook Yoo
Ann Pediatr Endocrinol Metab. 1997;2(2):233-240.

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A MERRF/MELAS Overlap Syndrome Associated with a New Point Mutation in the Mitochondrial DNA tRNA^Lys Gene
European Journal of Human Genetics. 1993;1(1):80-87   Crossref logo
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Impaired mitochondrial translation in human myoblasts harbouring the mitochondrial DNA tRNA lysine 8344 A → G (MERRF) mutation: relationship to proportion of mutant mitochondrial DNA
Journal of the Neurological Sciences. 1995;130(2):154-160   Crossref logo
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Erratum to “Impaired mitochondrial translation in human myoblasts harbouring the mitochondrial DNA tRNA lysine 8344 A → G (MERRF) mutation: relationship to proportion of mutant mitochondrial DNA”
Journal of the Neurological Sciences. 1995;132(1):95   Crossref logo
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MERRF family with 8344 mutation in tRNA (lys). Evidence of a mitochondrial vasculopathy in muscle biopsies
Neuromuscular Disorders. 1993;3(5-6):593-597   Crossref logo
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Familial Clustering Strongly Suggests that the Phenotypic Variation of the 8344 A>G Lys Mitochondrial tRNA Mutation is Encoded in cis
Annals of Human Genetics. 2012;76(4):296-300   Crossref logo
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Quantification of mitochondrial DNA and mitochondrial tRNA mutation at position 3243 in Korean gestational diabetes mellitus.
Fertility and Sterility. 2001;76(3):S158-S159   Crossref logo
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4121 Macular retinal dystrophy, deafness and diabetes mellitus, associated with a mutation of mitochondrial DNA (tRNA leu(3243)
Vision Research. 1995;35:S153   Crossref logo
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Two pathogenic mutations in the mitochondrial DNA tRNA Leu(UUR) gene (T3258C and A3280G) resulting in variable clinical phenotypes
Neuromuscular Disorders. 2003;13(5):416-420   Crossref logo
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MERRF/MELAS overlap syndrome associated with 3243 tRNALeu(UUR)mutation of mitochondrial DNA
Neuropathology. 1998;18(3):321-327   Crossref logo
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Screening for Mitochondrial tRNA Mutations in 318 Patients with Dilated Cardiomyopathy
Human Heredity. 2022;   Crossref logo
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