Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor

New England Journal of Medicine

Volumn 336, Issue 10, 1997, Pages 703-706

  Dunne, Mark J ^a   Kane, Charlotte ^a   Shepherd, Ruth M ^a   Sanchez, Jorge A ^d   James, Roger F L ^b   Johnson, Paul R V ^b   Aynsley Green, Albert ^c   Lu, Shan ^a,e   Clement IV, John P ^e   Lindley, Keith J ^c   Seino, Susumu ^d   Aguilar Bryan, Lydia ^e  

^a UNIVERSITY OF SHEFFIELD   (United Kingdom)

^b UNIVERSITY OF LEICESTER   (United Kingdom)

^c UNIVERSITY COLLEGE LONDON   (United Kingdom)

^d CHIBA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^e BAYLOR COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

INSULIN;

ARTICLE; CASE REPORT; CLINICAL FEATURE; CONSANGUINEOUS MARRIAGE; FAMILIAL DISEASE; FEMALE; GENETIC SUSCEPTIBILITY; HUMAN; HYPERINSULINEMIA; HYPOGLYCEMIA; INSULIN TREATMENT; PANCREAS RESECTION; PRESCHOOL CHILD; PRIORITY JOURNAL; RISK FACTOR;

ATP-BINDING CASSETTE TRANSPORTERS; FEMALE; HUMANS; HYPERINSULINISM; HYPOGLYCEMIA; INFANT, NEWBORN; INSULIN; ISLETS OF LANGERHANS; MUTATION; POTASSIUM CHANNELS; POTASSIUM CHANNELS, INWARDLY RECTIFYING; RECEPTORS, DRUG; SULFONYLUREA COMPOUNDS;

EID: 0031041271     PISSN: 00284793     EISSN: None     Source Type: Journal    
DOI: 10.1056/NEJM199703063361005     Document Type: Article

References (13)

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