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Mttl1 gene.c.A3243G

National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Restriction Enzymes ApaI Analysis to Find A3243G Mutation in Indonesia Diabetes Mellitus Type II Patients
The Use of PCR-RFLP (Polymerase Chain Reaction-Restriction Fragment Length Polymorphism) to find out the potential of… 
2012
2012
[Audiologic features of mitochondrial DNA A3243G mutation and its correlation with mutation rate].
OBJECTIVE To summarize the clinical audiologic features of patients with mitochondrial DNA (mtDNA) A3243G mutation and explore… 
2010
2010
Detection of eight frequently encountered point mutations in mitochondria in Chinese patients suggestive of mitochondrial encephalomyopathies.
2010
2010
Analysis of mtDNA A3243G mutation frequency in Hungary
The A3243G mutation in the mitochondrial tRNALeu (UUR) gene is one of the most common causes of mitochondrial DNA related… 
2010
2010
MELAS syndrome associated with both A3243G-tRNALeu mutation and multiple mitochondrial DNA deletions
2007
2007
Valproic Acid Aggravates Epilepsy due to MELAS in a Patient with an A3243G Mutation of Mitochondrial DNA
Epilepsy is one of the most common presentations of patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and… 
2006
2006
A Case of Melas (A3243G) on Chronic Dichloroacetate Treatment
eralized epileptic dysfunction, more marked in the right regions, and phenytoin was started. Mild perceptive deafness was also… 
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