Associated Papers
A survey on mutation spectrum in Iranian patients with limb-girdle muscular dystrophies.
Khalilian S et al.
Human Genomics, 2025
Broadening the paradigm of laminin α2-related muscular dystrophy: A case of partial merosin deficiency with compound heterozygous variants.
Tavasoli A et al.
Sage Open Medical Case Reports, 2025
Reviewing Large LAMA2 Deletions and Duplications in Congenital Muscular Dystrophy Patients.
Oliveira J et al.
Journal of Neuromuscular Diseases, 0
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