Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: Association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11

American Journal of Pathology

Volumn 158, Issue 6, 2001, Pages 2177-2184

  Fournet, Jean Christophe ^a,b   Mayaud, Christine ^a   De Lonlay, Pascale ^b   Gross Morand, Marie Sylvie ^a   Verkarre, Virginie ^a,b   Castanet, Mireille ^a   Devillers, Martine ^a   Rahier, Jacques ^c   Brunelle, Francis ^b   Robert, Jean Jacques ^b   Nihoul Fékété, Claire ^b   Saudubray, Jean Marie ^b   Junien, Claudine ^a,b  

^a INSERM   (France)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

^c CLINIQUES UNIVERSITAIRES SAINT LUC   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; POTASSIUM CHANNEL; PROTEIN ABCC8; PROTEIN KCNJ11; SULFONYLUREA RECEPTOR; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; CHROMOSOME 11P; CHROMOSOME LOSS; CLINICAL ARTICLE; CONTROLLED STUDY; GENE EXPRESSION; GENE MUTATION; GENETIC ASSOCIATION; GENETIC CODE; GROWTH RATE; HOMOZYGOSITY; HUMAN; HYPERINSULINEMIA; HYPERINSULINISM; HYPERPLASIA; HYPOGLYCEMIA; INSULIN RELEASE; MITOSIS; PANCREAS ADENOMA; PANCREAS ISLET; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

EID: 0034970925     PISSN: 00029440     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9440(10)64689-5     Document Type: Article

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