Mttl1 gene.c.A3243G

 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2004-2012
01220042012

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2012
2012
OBJECTIVE To summarize the clinical audiologic features of patients with mitochondrial DNA (mtDNA) A3243G mutation and explore… (More)
Is this relevant?
2010
2010
The syndrome of mitochondrial encephalopathy, lactic acidosis, and stroke-like episode (MELAS) is characterized clinically by… (More)
Is this relevant?
2006
2006
Epilepsy is one of the most common presentations of patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and… (More)
  • figure 1
  • figure 2
Is this relevant?
2006
2006
eralized epileptic dysfunction, more marked in the right regions, and phenytoin was started. Mild perceptive deafness was also… (More)
  • figure 1
  • table 1
Is this relevant?
Highly Cited
2004
Highly Cited
2004
BACKGROUND The A3243G mitochondrial tRNA leu(UUR) point mutation causes mitochondrial myopathy, encephalopathy, lactic acidosis… (More)
  • table 1
  • figure 1
  • figure 2
  • figure 3
Is this relevant?