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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
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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
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2007
2007
Epilepsy is one of the most common presentations of patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and… Expand
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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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