Complete glucokinase deficiency is not a common cause of permanent neonatal diabetes [3]

Diabetologia

Volumn 45, Issue 2, 2002, Pages 290-

  Gloyn, A L ^a  

^a UNIVERSITY OF EXETER   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DNA; GLUCOKINASE; GLUCOSE;

CLINICAL ARTICLE; DIABETOGENESIS; ENZYME DEFICIENCY; GENE FREQUENCY; GENE MUTATION; GLUCOSE METABOLISM; HUMAN; LETTER; MATURITY ONSET DIABETES MELLITUS; NEWBORN DIABETES MELLITUS; NEWBORN DISEASE; PRIORITY JOURNAL;

DIABETES MELLITUS; DIABETES MELLITUS, TYPE 2; GLUCOKINASE; HOMOZYGOTE; HUMANS; INFANT, NEWBORN; INFANT, NEWBORN, DISEASES; PREVALENCE;

EID: 18344385482     PISSN: 0012186X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00125-001-0746-9     Document Type: Letter

References (8)

1. Neonatal diabetes
2. Long-term course of neonatal diabetes
3. Transient neonatal diabetes: Widening the understanding of the etiopathogenesis of diabetes
4. EIF2AK3, encoding translation initiation factor 2-a kinase, is mutated in patients with Wolcott-Rallison syndrome
5. X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy
6. Neonatal diabetes mellitus due to complete glucokinase deficiency
7. Familial hyperglycaemia due to mutations in glucokinase: Definition of a subject of diabetes mellitus
8. A high prevalence of glucokinase mutations in gestational diabetic subjects selected by clinical criteria