MYH2 myopathy, a new case expands the clinical and pathological spectrum of the recessive form

ConclusionThis report contributes to expand the clinical and genetic spectrum ofMYH2 myopathies and to increase the awareness of these very rare diseases.

Source: Molecular Genetics & Genomic Medicine - June 23, 2020 Category: Genetics & Stem Cells Authors: Roberta Telese, Serena Pagliarani, Alberto Lerario, Patrizia Ciscato, Gigliola Fagiolari, Denise Cassandrini, Nadia Grimoldi, Giorgio Conte, Claudia Cinnante, Filippo M. Santorelli, Giacomo P. Comi, Monica Sciacco, Lorenzo Peverelli Tags: CLINICAL REPORT Source Type: research