The molecular basis for familial persistent hyperinsulinemic hypoglycemia of infancy.

Proceedings of the Association of American Physicians

Volumn 108, Issue 1, 1996, Pages 14-19

  Thomas, P M ^a   Cote, G J ^a   Wohllk, N ^a   Mathew, P M ^a   Gagel, R F ^a  

^a UNIVERSITY OF TEXAS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER; DRUG RECEPTOR; INSULIN; INWARDLY RECTIFYING POTASSIUM CHANNEL; POTASSIUM CHANNEL; SULFONYLUREA DERIVATIVE; SULFONYLUREA RECEPTOR;

ARTICLE; FEMALE; GENETICS; HUMAN; HYPERINSULINISM; HYPOGLYCEMIA; INFANT; MALE; METABOLISM; NUCLEOTIDE SEQUENCE; PEDIGREE; POINT MUTATION; RESTRICTION MAPPING; SECRETION;

ATP-BINDING CASSETTE TRANSPORTERS; DNA MUTATIONAL ANALYSIS; FEMALE; HUMANS; HYPERINSULINISM; HYPOGLYCEMIA; INFANT; INSULIN; MALE; PEDIGREE; POINT MUTATION; POTASSIUM CHANNELS; POTASSIUM CHANNELS, INWARDLY RECTIFYING; RECEPTORS, DRUG; RESTRICTION MAPPING; SULFONYLUREA COMPOUNDS;

EID: 0029683205     PISSN: 1081650X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)