Related Experiment Video

Updated: Aug 7, 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

[Weill-Marchesani's syndrome: familial involvement]

C Veiga de la Jara1, J Bosch Valero, E Torres Suárez

  • 1Hospital Universitario Ramón y Cajal, Madrid, España. veigajara@hotmail.com

Archivos De La Sociedad Espanola De Oftalmologia
|June 29, 2006
PubMed
Abstract

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