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The ties that bind: functional clusters in limb-girdle muscular dystrophy, Skeletal Muscle
Glycogenin-1 deficiency mimicking limb-girdle muscular dystrophy - ScienceDirect
limb girdle muscular dystrophy 1F (LGMD1F) - News, Articles, Whitepapers - Drug Target Review
Paving the way for future gene therapies: A case study of scientific spillover from delandistrogene moxeparvovec - ScienceDirect
Limb-Girdle Muscular Dystrophy Leaders Advance Collaborative Dialogue to Accelerate Drug Development to Address the Urgent Unmet Need in Limb-Girdle Muscular Dystrophy
LGMD2L Foundation
Limb girdle muscular dystrophy type 2G with myopathic-neurogenic motor unit potentials and a novel muscle image pattern, BMC Clinical Pathology
A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21
PDF) A Journey with LGMD: From Protein Abnormalities to Patient Impact
Neuromuscular Disorders: A Histomorphological and Clinicopathological Evaluation in a Tertiary Care Centre
Autosomal recessive LGMD. Comparison of the nomenclature in 1995 to the
Genes, Free Full-Text
The muscular dystrophies (Chapter 11) - Neurogenetics