Genetic heterogeneity of myoclonus epilepsy with ragged-red fibers syndrome
Author:
Publisher
Wiley
Subject
Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology
Reference8 articles.
1. The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome.
2. The 3243 MELAS Mutation in a Pedigree with MERRF
3. Clinicopathological features of MERRF
4. Tissue-specific selection for different mtDNA genotypes in heteroplasmic mice
5. Myoclonus epilepsy associated with ragged-red fibers: A G-to-A mutation at nucleotide pair 8363 in mitochondrial tRNALys in two families
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Genetic, pathogenetic, and phenotypic implications of the mitochondrial A3243G tRNALeu(UUR) mutation;Acta Neurologica Scandinavica;2007-07
2. Central nervous system manifestations of mitochondrial disorders;Acta Neurologica Scandinavica;2006-10
3. Bilateral Putaminal Necrosis Associated With the Mitochondrial DNA A8344G Myoclonus Epilepsy With Ragged Red Fibers (MERRF) Mutation: An Infantile Case;Journal of Child Neurology;2006-01
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