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Mttl1 gene.c.A3243G

National Institutes of Health

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2015
2015
The Use of PCR-RFLP (Polymerase Chain Reaction-Restriction Fragment Length Polymorphism) to find out the potential of… Expand
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2012
2012
OBJECTIVE To summarize the clinical audiologic features of patients with mitochondrial DNA (mtDNA) A3243G mutation and explore… Expand
2010
2010
To evaluate eight frequently encountered mitochondrial DNA (mtDNA) point mutations (A3243G, T8993G/C, A8344G, A1555G, G11778A… Expand
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2010
2010
The A3243G mutation in the mitochondrial tRNALeu (UUR) gene is one of the most common causes of mitochondrial DNA related… Expand
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2010
2010
The syndrome of mitochondrial encephalopathy, lactic acidosis, and stroke-like episode (MELAS) is characterized clinically by… Expand
2007
2007
Epilepsy is one of the most common presentations of patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and… Expand
2006
2006
Epilepsy is one of the most common presentations of patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and… Expand
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2006
2006
eralized epileptic dysfunction, more marked in the right regions, and phenytoin was started. Mild perceptive deafness was also… Expand
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Highly Cited
2004
Highly Cited
2004
BACKGROUND The A3243G mitochondrial tRNA leu(UUR) point mutation causes mitochondrial myopathy, encephalopathy, lactic acidosis… Expand
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