Further evidence for a dominant form of familial persistent hyperinsulinemic hypoglycemia of infancy: A family with documented hyperinsulinemia in two generations [3]

Journal of Clinical Endocrinology and Metabolism

Volumn 83, Issue 6, 1998, Pages 2215-2216

  Hufnagel, M ^a   Eichmann, D ^a   Stieh, J ^a   Santer, R ^a  

^a UNIVERSITY HOSPITAL SCHLESWIG HOLSTEIN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CONSANGUINEOUS MARRIAGE; DISEASE CLASSIFICATION; GENE LOCUS; HUMAN; HUMAN CELL; HUMAN TISSUE; HYPERINSULINEMIA; HYPERINSULINISM; HYPOGLYCEMIA; INFANT; INFANT DISEASE; INSULIN RELEASE; LETTER; PEDIGREE; PRIORITY JOURNAL;

ATP-BINDING CASSETTE TRANSPORTERS; FEMALE; HUMANS; HYPERINSULINISM; HYPOGLYCEMIA; INFANT; MUTATION; PEDIGREE; POTASSIUM CHANNELS; POTASSIUM CHANNELS, INWARDLY RECTIFYING; RECEPTORS, DRUG;

EID: 0031787335     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.83.6.2215     Document Type: Letter

References (5)