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PMID: 17300999 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Population prevalence of the MELAS A3243G mutation.

Mitochondrion ·Vol. 7 ·No. 3 ·2007-05-00 ·Pages 230-3

Manwaring N, Jones MM, Wang JJ, Rochtchina E, Howard C, Mitchell P, Sue CM

Abstract

We aimed to establish the population prevalence of the MELAS 3243A>G mtDNA mutation in a large Caucasian-based population (n=2954; 99% Caucasian, 57% women and mean age of 66.4 years). All participants underwent comprehensive clinical evaluation including audiologic testing. We detected the 3243A>G mutation in seven subjects using standard polymerase chain reaction/restriction fragment length polymorphism methods, establishing a population prevalence of 236/100000 (0.24%; 95% CI 0.10-0.49%); much higher than previously reported. All had mild to moderate hearing loss. Our findings indicate that subjects with the 3243A>G mtDNA mutation could be markedly under-recognised in the community.

MeSH Terms
Adult Aged Aged, 80 and over Australia/epidemiology DNA, Mitochondrial/genetics Female Humans MELAS Syndrome/epidemiology,genetics Male Middle Aged Mutation Polymorphism, Single Nucleotide Prevalence
Chemicals
DNA, Mitochondrial
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Manwaring Neil
Kolling Institute, Department of Neurogenetics, University of Sydney, Clinic 4, Royal North Shore Hospital, Reserve Road, St. Leonards, NSW 2065, Australia.
Jones Michael M
Wang Jie Jin
Rochtchina Elena
Howard Chris
Mitchell Paul
Sue Carolyn M
Article Info
Journal
Mitochondrion
Abbr.
Mitochondrion
ISSN
1567-7249
Published
2007-05-00
Epub
2007-00-08
Pages
230-3
Language
English
Region
Netherlands
NLM ID
100968751
Subset
IM
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