A novel unstable mutation in mitochondrial DNA responsible for maternally inherited diabetes and deafness

Diabetes Care

Volumn 34, Issue 12, 2011, Pages 2591-2593

  Bannwarth, Sylvie ^a,b   Abbassi, Meriame ^b,c   Valéro, René ^d   Fragaki, Konstantina ^a,b   Dubois, Noémie ^d   Vialettes, Bernard ^d   Paquis Flucklinger, Véronique ^a,b  

^a CENTRE HOSPITALIER UNIVERSITAIRE DE NICE   (France)

^b UNIVERSITÉ CÔTE D'AZUR   (France)

^c MOHAMMED V UNIVERSITY   (Morocco)

^d TIMONE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADENINE; BRAIN NATRIURETIC PEPTIDE; CREATININE; DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; FUROSEMIDE; GUANOSINE; HEMOGLOBIN A1C; INSULIN; ISOPHANE INSULIN; MITOCHONDRIAL DNA; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE);

AGED; ARTICLE; CASE REPORT; CREATININE BLOOD LEVEL; DNA SEQUENCE; FIBROBLAST; GENE INSERTION; GENE MUTATION; GENETIC CODE; GENOMIC INSTABILITY; HETEROPLASMY; HUMAN; MALE; MATERNALLY INHERITED DIABETES AND DEAFNESS; OXIDATIVE PHOSPHORYLATION; PHENOTYPE; RESPIRATORY CHAIN; STOP CODON; WESTERN BLOTTING; DISORDERS OF MITOCHONDRIAL FUNCTIONS; GENETICS; HEARING IMPAIRMENT; NON INSULIN DEPENDENT DIABETES MELLITUS; NUCLEOTIDE SEQUENCE; PEDIGREE; POINT MUTATION;

AGED; BASE SEQUENCE; DEAFNESS; DIABETES MELLITUS, TYPE 2; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT COMPLEX I; HUMANS; MALE; MITOCHONDRIAL DISEASES; PEDIGREE; POINT MUTATION;

EID: 84859865028     PISSN: 01495992     EISSN: 19355548     Source Type: Journal    
DOI: 10.2337/dc11-1012     Document Type: Article

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