Related Experiment Video

Updated: Jun 4, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
03:45

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

Published on: August 8, 2022

Four cases of Muckle-Wells syndrome within the same family

Ana Francisca Junqueira Ribeiro Pereira1, Luciana Baptista Pereira, Everton Carlos Siviero do Vale

  • 1Dermatological Service, University Hospital of the Federal University of Minas Gerais, Belo Horizonte, MG, Brasil. anafranciscajunqueira@hotmail.com

Anais Brasileiros De Dermatologia
|February 11, 2011
PubMed

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