Calcium Mechanisms in Limb-Girdle Muscular Dystrophy with CAPN3 Mutations.

Volume: 20, Issue: 18, Pages: 4548
Published: Sep 13, 2019
Abstract
Limb-girdle muscular dystrophy recessive 1 (LGMDR1), previously known as LGMD2A, is a rare disease caused by mutations in the CAPN3 gene. It is characterized by progressive weakness of shoulder, pelvic, and proximal limb muscles that usually appears in children and young adults and results in loss of ambulation within 20 years after disease onset in most patients. The pathophysiological mechanisms involved in LGMDR1 remain mostly unknown, and to...
Paper Details
Title
Calcium Mechanisms in Limb-Girdle Muscular Dystrophy with CAPN3 Mutations.
Published Date
Sep 13, 2019
Volume
20
Issue
18
Pages
4548
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