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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

Published on: August 8, 2022

HNF1alpha mutations are present in half of clinically defined MODY patients in South-Brazilian individuals

Jorge de Faria Maraschin1, Caroline Kannengiesser, Nádia Murussi

  • 1Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.

Arquivos Brasileiros De Endocrinologia E Metabologia
|January 27, 2009
PubMed

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