Myocardial strain analysis using cardiac magnetic resonance in patients with calpainopathy

Limb –girdle muscular dystrophy (LGMD) is a genetically and clinically heterogeneous group of rare muscular dystrophies. Subtype 2A (LGMD2A) also known as “calpainopathy” is an inherited autosomal recessive gen...

Source: Orphanet Journal of Rare Diseases - April 30, 2021 Category: Internal Medicine Authors: Silvio Quick, Max Winkler, Uwe Speiser, Karim Ibrahim, Jochen Sch äfer, Axel Linke, Kun Zhang, Marian Christoph and Felix M. Heidrich Tags: Research Source Type: research