Mutations in the ABCC8 gene can cause autoantibody-negative insulin-dependent diabetes

Diabetes and Metabolism

Volumn 35, Issue 3, 2009, Pages 233-235

  Hartemann Heurtier, A ^a,b   Simon, A ^c   Bellanne Chantelot C ^d   Reynaud, R ^e   Cave H ^f   Polak, M ^c,g,h   Vaxillaire, M ⁱ   Grimaldi, A ^a,b  

^a PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^b SORBONNE UNIVERSITÉ   (France)

^c HÔPITAL NECKER ENFANTS MALADES   (France)

^d ASSISTANCE PUBLIQUE HÔPITAUX DE PARIS   (France)

^e TIMONE HOSPITAL   (France)

^f HÔPITAL ROBERT DEBRÉ   (France)

^g UNIVERSITÉ PARIS DESCARTES   (France)

^h INSERM   (France)

ⁱ CNRS   (France)

Author keywords

ABCC8 mutation; Insulin dependent diabetes; Sulphonylurea

Indexed keywords

AUTOANTIBODY; C PEPTIDE; GLIBENCLAMIDE; HEMOGLOBIN A1C; INSULIN; SULFONYLUREA;

ABCC8 GENE; ADULT; ANAMNESIS; ARTICLE; BODY MASS; CASE REPORT; CHRONIC KIDNEY FAILURE; DIABETES MELLITUS; DIABETIC PATIENT; DIABETIC RETINOPATHY; DRUG WITHDRAWAL; ECHOGRAPHY; FEMALE; GENE; GENE MUTATION; GLUCOSE BLOOD LEVEL; HETEROZYGOTE; HUMAN; INFANT; INSULIN DEPENDENT DIABETES MELLITUS; MALE; PHENOTYPE; POLYDIPSIA; POLYURIA; PROTEINURIA;

ADOLESCENT; ADULT; ATP-BINDING CASSETTE TRANSPORTERS; AUTOANTIBODIES; DIABETES MELLITUS, TYPE 1; FEMALE; HEPATOCYTE NUCLEAR FACTOR 1-ALPHA; HUMANS; INFANT, NEWBORN; INFANT, NEWBORN, DISEASES; MALE; MIDDLE AGED; MUTATION; POTASSIUM CHANNELS, INWARDLY RECTIFYING; RECEPTORS, DRUG;

EID: 67349088441     PISSN: 12623636     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.diabet.2009.01.003     Document Type: Article

References (10)

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