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Updated: Jul 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

A glycine-valine substitution in alpha2 type V procollagen associated with recurrent cervical artery dissection

Christiane Wagner, Manja Kloss, Christoph Lichy

    Journal of Neurology
    |June 26, 2008
    PubMed
    Abstract

    No abstract available in PubMed .

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