Diabetes and deafness: is it sufficient to screen for the mitochondrial 3243A>G mutation alone?
Diabetes Care
.
2007 Sep;30(9):2238-9.
doi: 10.2337/dc07-0466.
Epub 2007 May 31.
Authors
Roger G Whittaker
1
,
Andrew M Schaefer
,
Robert McFarland
,
Robert W Taylor
,
Mark Walker
,
Douglass M Turnbull
Affiliation
1
Mitochondrial Research Group, School of Neurology, Neurobiology and Psychiatry, Newcastle University, Newcastle upon Tyne, UK.
[email protected]
PMID:
17540956
DOI:
10.2337/dc07-0466
No abstract available
MeSH terms
DNA, Mitochondrial / genetics*
Deafness / genetics*
Diabetes Complications / genetics*
Genes, Mitochondrial
Genetic Testing
Humans
Mitochondrial Diseases / genetics*
Point Mutation
Retrospective Studies
Substances
DNA, Mitochondrial
Grants and funding
074454/WT_/Wellcome Trust/United Kingdom
G108/539/MRC_/Medical Research Council/United Kingdom