Glucokinase gene mutations are not a common cause of permanent neonatal diabetes in France [3]

Diabetologia

Volumn 45, Issue 3, 2002, Pages 454-455

  Vaxillaire, Martine ^a   Samson, C ^a   Cave H ^a   Metz, C ^a   Froguel, P ^a   Polak, M ^a  

^a INSTITUT PASTEUR DE LILLE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

GLUCOKINASE; INSULIN;

CHROMOSOME 6; CONSANGUINITY; DIABETES MELLITUS; EXON; FRANCE; GENE MUTATION; GENETIC ASSOCIATION; GENETIC SCREENING; GLUCOSE BLOOD LEVEL; GLUCOSE INTOLERANCE; HUMAN; INFANT; INSULIN RELEASE; INSULIN TREATMENT; INTRAUTERINE GROWTH RETARDATION; LETTER; NEWBORN; NEWBORN DISEASE; PANCREAS ISLET BETA CELL; PRIORITY JOURNAL;

ADOLESCENT; DIABETES MELLITUS; FRANCE; GLUCOKINASE; GLUCOSE INTOLERANCE; HUMANS; HYPERGLYCEMIA; INFANT, NEWBORN; MUTATION; PARENTS;

EID: 0036204854     PISSN: 0012186X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00125-001-0741-1     Document Type: Letter

References (8)

1. Aetiopathology and genetic basis of neonatal diabetes
2. Transient neonatal diabetes: Widening the understanding of the etiopathogenesis of diabetes
3. Refinement of the 6q chromosomal region implicated in transient neonatal diabetes
4. A conserved imprinting control region at the HYMAI/ZAC domain is implicated in transient neonatal diabetes mellitus
5. Neonatal diabetes mellitus due to complete glucokinase deficiency
6. Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families
7. Human glucokinase gene: Isolation, characterization, and identification of two missense mutations linked to early-onset non-insulin-dependent (type 2) diabetes mellitus
8. Routine mutation screening of HNF-1alpha and GCK genes in MODY diagnosis: How effective are the techniques of DHPLC and direct sequencing used in combination?