Rapid and Sensitive Real-Time Polymerase Chain Reaction Method for Detection and Quantification of 3243A>G Mitochondrial Point Mutation

Maternally inherited diabetes and deafness and mitochondrial encephalomyopathy, lactic acidosis with stroke-like episodes result from the 3243A>G mitochondrial point mutation. Current methods to detect the presence of the mutation have limited sensitivity and may lead to potential misclassificati...

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Detalles Bibliográficos
Main Authors: Singh, Rinki, Ellard, Sian, Hattersley, Andrew, Harries, Lorna W.
Formato: Artigo
Idioma:Inglês
Publicado: American Society for Investigative Pathology 2006
Assuntos:
Regular Articles
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC1867583/
https://ncbi.nlm.nih.gov/pubmed/16645209
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2353/jmoldx.2006.050067
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