Low prevalence of MODY2 and MODY3 mutations in Brazilian individuals with clinical MODY phenotype.

Abstract:

:Prevalence of MODY2 and MODY3 mutations has been assessed in 23 Brazilian families with MODY phenotype. Mutations in HNF-1alpha have been found in 3 families (13%) and 2 families (8.7%) had new glucokinase mutations. These genes do not explain the majority of MODY cases in Brazilian population.

authors

Furuzawa GK,Giuffrida FM,Oliveira CS,Chacra AR,Dib SA,Reis AF

doi

10.1016/j.diabres.2008.06.011

subject

Has Abstract

pub_date

2008-09-01 00:00:00

pages

e12-4

issue

3

eissn

0168-8227

issn

1872-8227

pii

S0168-8227(08)00280-5

journal_volume

81

pub_type

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