RGD Reference Report - Familial hyperinsulinism caused by an activating glucokinase mutation. - Rat Genome Database

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Familial hyperinsulinism caused by an activating glucokinase mutation.

Authors: Glaser, B  Kesavan, P  Heyman, M  Davis, E  Cuesta, A  Buchs, A  Stanley, CA  Thornton, PS  Permutt, MA  Matschinsky, FM  Herold, KC 
Citation: Glaser B, etal., N Engl J Med. 1998 Jan 22;338(4):226-30.
RGD ID: 1601294
Pubmed: PMID:9435328   (View Abstract at PubMed)
DOI: DOI:10.1056/NEJM199801223380404   (Journal Full-text)

Abstract for this paper unavailable

RGD Manual Disease Annotations    Click to see Annotation Detail View
TermQualifierEvidenceWithReferenceNotesSourceOriginal Reference(s)
hyperinsulinism  IAGP 1601294hyperinsulinemic hypoglycemia more ...RGD 
hyperinsulinism  ISOGCK (Homo sapiens)1601294; 1601294hyperinsulinemic hypoglycemia more ...RGD 
hypoglycemia  IAGP 1601294hyperinsulinemic hypoglycemia more ...RGD 
hypoglycemia  ISOGCK (Homo sapiens)1601294; 1601294hyperinsulinemic hypoglycemia more ...RGD 

Objects Annotated

Genes (Rattus norvegicus)
Gck  (glucokinase)

Genes (Mus musculus)
Gck  (glucokinase)

Genes (Homo sapiens)
GCK  (glucokinase)


Additional Information