An autosomal dominant form of familial persistent hyperinsulinemic hypoglycemia of infancy, not linked to the sulfonylurea receptor locus

Journal of Clinical Endocrinology and Metabolism

Volumn 82, Issue 4, 1997, Pages 1192-1194

  Kukuvitis, Asterios ^a   Deal, Cheri ^b   Arbour, Laura ^a   Polychronakos, Constantin ^a,c  

^a RESEARCH INSTITUTE OF THE MCGILL UNIVERSITY HEALTH CENTRE   (Canada)

^b UNIVERSITY OF MONTREAL   (Canada)

^c MONTREAL CHILDREN S HOSPITAL   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

GLUCOKINASE; GLUCOSE; INSULIN; SULFONYLUREA;

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CANADA; CLINICAL ARTICLE; FAMILIAL DISEASE; FEMALE; GENE CLUSTER; GENE LOCUS; GENE MUTATION; GENETIC HETEROGENEITY; GENETIC LINKAGE; GLUCOSE BLOOD LEVEL; HUMAN; HUMAN CELL; HYPERINSULINEMIA; HYPOGLYCEMIA; INFANT; INSULIN RELEASE; MALE; NEGATIVE FEEDBACK; PRIORITY JOURNAL; RECEPTOR GENE;

AGED; ALLELES; ATP-BINDING CASSETTE TRANSPORTERS; CHROMOSOME MAPPING; FEMALE; GENES, DOMINANT; GENOTYPE; HUMANS; HYPERINSULINISM; HYPOGLYCEMIA; INFANT; INFANT, NEWBORN; LINKAGE (GENETICS); MALE; PEDIGREE; POTASSIUM CHANNELS; POTASSIUM CHANNELS, INWARDLY RECTIFYING; RECEPTORS, DRUG; SULFONYLUREA COMPOUNDS;

EID: 0030936044     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.82.4.1192     Document Type: Article

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