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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
5
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pubmed:dateCreated |
2000-8-1
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pubmed:abstractText |
The mitochondrial DNA A to G mutation at nucleotide 3243 (mt3243) is associated with a subtype of diabetes characterized by maternal transmission and deafness. We have previously reported a 2.7% prevalence of this mutation in a cohort of young patients with either type 1 or type 2 diabetes. In this study, we aimed to confirm this finding by examining for the prevalence of this mutation in a large-scale study.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
|
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0300-0664
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
52
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
557-64
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pubmed:dateRevised |
2011-1-11
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pubmed:meshHeading |
pubmed-meshheading:10792334-Adult,
pubmed-meshheading:10792334-Age of Onset,
pubmed-meshheading:10792334-Aged,
pubmed-meshheading:10792334-Asian Continental Ancestry Group,
pubmed-meshheading:10792334-C-Peptide,
pubmed-meshheading:10792334-Case-Control Studies,
pubmed-meshheading:10792334-Chi-Square Distribution,
pubmed-meshheading:10792334-DNA, Mitochondrial,
pubmed-meshheading:10792334-Diabetes Mellitus, Type 2,
pubmed-meshheading:10792334-Female,
pubmed-meshheading:10792334-Hong Kong,
pubmed-meshheading:10792334-Humans,
pubmed-meshheading:10792334-Male,
pubmed-meshheading:10792334-Middle Aged,
pubmed-meshheading:10792334-Pedigree,
pubmed-meshheading:10792334-Point Mutation,
pubmed-meshheading:10792334-Polymerase Chain Reaction
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pubmed:year |
2000
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pubmed:articleTitle |
Mitochondrial DNA A3243G mutation in patients with early- or late-onset type 2 diabetes mellitus in Hong Kong Chinese.
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pubmed:affiliation |
Department of Medicine, The Chinese University of Hong Kong, Prince of Wales Hospital, Shatin, Hong Kong. maggieng@cuhk.edu.hk
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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