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Volumn 17, Issue 12, 2000, Pages 841-847
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HLA-DQ polymorphism and degree of heteroplasmy of the A3243G mitochondrial DNA mutation in maternally inherited diabetes and deafness
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Author keywords
Autoimmunity; Genetics; HLA; Maternally inherited diabetes and deafness; Mitochondria; Type 1 diabetes mellitus; Type 2 diabetes mellitus
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Indexed keywords
HLA DQ ANTIGEN;
MITOCHONDRIAL DNA;
ADULT;
ARTICLE;
CLINICAL ARTICLE;
CONTROLLED STUDY;
DIABETES MELLITUS;
DISEASE ASSOCIATION;
DISEASE PREDISPOSITION;
EXTRACHROMOSOMAL INHERITANCE;
GENETIC POLYMORPHISM;
HEARING IMPAIRMENT;
HUMAN;
INSULIN DEPENDENT DIABETES MELLITUS;
LEUKOCYTE;
NON INSULIN DEPENDENT DIABETES MELLITUS;
PHENOTYPE;
ADOLESCENT;
ADULT;
AGED;
DEAFNESS;
DIABETES COMPLICATIONS;
DIABETES MELLITUS;
DIABETES MELLITUS, TYPE 1;
DIABETES MELLITUS, TYPE 2;
DNA MUTATIONAL ANALYSIS;
DNA, MITOCHONDRIAL;
HETEROZYGOTE DETECTION;
HLA-DQ ANTIGENS;
HUMANS;
LEUKOCYTES;
MIDDLE AGED;
MOUTH MUCOSA;
MUTATION;
PHENOTYPE;
POLYMORPHISM, GENETIC;
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EID: 0034521838
PISSN: 07423071
EISSN: None
Source Type: Journal
DOI: 10.1046/j.1464-5491.2000.00379.x Document Type: Article |
Times cited : (26)
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References (32)
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