Prevalence of maturity-onset diabetes of the young mutations in Brazilian families with autosomal-dominant early-onset type 2 diabetes [2]

Diabetes Care

Volumn 24, Issue 4, 2001, Pages 786-788

  Moisés, Regina S ^a   Reis, André F ^a,b   Morel, Valérie ^c   Chacra, Antônio R ^a   Dib, Sérgio A ^a   Bellanné Chantelot, Christine ^c   Velho, Gilberto ^b,d  

^a FEDERAL UNIVERSITY OF SÃO PAULO   (Brazil)

^b INSERM   (France)

^c FONDATION JEAN DAUSSET CEPH   (France)

^d HÔPITAL SAINT VINCENT DE PAUL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

GLUCOKINASE; HEPATOCYTE NUCLEAR FACTOR 4; NUCLEAR FACTOR I;

ADOLESCENT; ADULT; AUTOSOMAL DOMINANT DISORDER; BRAZIL; CLINICAL ARTICLE; FAMILIAL DISEASE; FEMALE; GENE MUTATION; HUMAN; JUVENILE DIABETES MELLITUS; LETTER; MALE; MATURITY ONSET DIABETES MELLITUS; NON INSULIN DEPENDENT DIABETES MELLITUS; PREVALENCE;

EID: 0034833668     PISSN: 01495992     EISSN: None     Source Type: Journal    
DOI: 10.2337/diacare.24.4.786     Document Type: Letter

References (7)

1. Mutation screening in 18 Caucasian families suggests the existence of other MODY genes
2. Maturity onset diabetes of the young: Clinical heterogeneity explained by genetic heterogeneity
3. Molecular genetics of MODY in Germany
4. High frequency of mutations in MODY and mitochondrial genes in Scandinavian patients with familial early-onset diabetes
5. Missense mutations in the insulin promoter factor-1 gene predispose to type 2 diabetes
6. Mutations in the hepatocyte nuclear factor-1α gene in MODY and early-onset NIDDM: Evidence for a mutational hotspot in exon 4
7. Missense mutations in the human insulin promoter factor-1 gene and their relation to maturity-onset diabetes of the young and late-onset type 2 diabetes mellitus in Caucasians