Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene

Diabetes

Volumn 48, Issue 8, 1999, Pages 1652-1657

  Glaser, Benjamin ^a,d   Ryan, Fergus ^b   Donath, Marc ^a   Landau, Heddy ^a   Stanley, Charles A ^c   Baker, Lester ^c   Barton, David E ^b   Thornton, Paul S ^b  

^a HEBREW UNIVERSITY   (Israel)

^b OUR LADY S CHILDREN S HOSPITAL   (Ireland)

^c CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^d HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

INSULIN; SULFONYLUREA RECEPTOR;

ADULT; APOPTOSIS; ARTICLE; CASE REPORT; DISEASE SEVERITY; GENE MUTATION; GENOTYPE; GERM LINE; HOMOZYGOSITY; HUMAN; HUMAN CELL; HYPERINSULINISM; INSULIN RELEASE; MALE; PANCREAS ISLET BETA CELL; PATHOPHYSIOLOGY; PRIORITY JOURNAL; RECESSIVE INHERITANCE;

ALLELES; APOPTOSIS; ATP-BINDING CASSETTE TRANSPORTERS; CHROMOSOMES, HUMAN, PAIR 11; FATHERS; GENE DELETION; GENES, RECESSIVE; HOMOZYGOTE; HUMANS; HYPERINSULINISM; HYPERPLASIA; INFANT; INFANT, NEWBORN; ISLETS OF LANGERHANS; MALE; MOTHERS; MUTATION; POTASSIUM CHANNELS; POTASSIUM CHANNELS, INWARDLY RECTIFYING; RECEPTORS, DRUG;

EID: 0032790274     PISSN: 00121797     EISSN: None     Source Type: Journal    
DOI: 10.2337/diabetes.48.8.1652     Document Type: Article

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