Disease: Muscular dystrophy- limb-girdle- type 1A
- A cryptic intronic LAMA2 insertion in a boy with mild congenital muscular dystrophy type 1A
- A novel <em>de novo</em> variant of <em>LAMA2</em> contributes to merosin deficient congenital muscular dystrophy type 1A: Case report
- ANO5 mutations in the Polish limb girdle muscular dystrophy patients: Effects on the protein structure
- Circulating Biomarkers in Muscular Dystrophies: Disease and Therapy Monitoring
- Compound heterozygous c.598_612del and c.1746-20C > G CAPN3 genotype cause autosomal recessive limb-girdle muscular dystrophy-1: a case report
- Four new Finnish families with LGMD1D; refinement of the clinical phenotype and the linked 7q36 locus
- Involvement of muscle satellite cell dysfunction in neuromuscular disorders: Expanding the portfolio of satellite cell-opathies
- Limb girdle muscular dystrophy 23 caused by compound heterozygous mutations of <em>LAMA2</em> gene
- Limb girdle muscular dystrophy due to <em>LAMA2</em> gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosis
- Muscle magnetic resonance imaging in patients with LAMA2-related muscular dystrophy
- Novel mutation identification and copy number variant detection via exome sequencing in congenital muscular dystrophy
- Quantitative Muscle MRI in Patients with Neuromuscular Diseases-Association of Muscle Proton Density Fat Fraction with Semi-Quantitative Grading of Fatty Infiltration and Muscle Strength at the Thigh Region
- Recent advancements in exon-skipping therapies using antisense oligonucleotides and genome editing for the treatment of various muscular dystrophies
- Somatic and germinal mosaicism in a Han Chinese family with laminopathies
- Treatment with galectin-1 improves myogenic potential and membrane repair in dysferlin-deficient models
- Tripartite motif-containing protein 32 regulates Ca<sup>2+</sup> movement in skeletal muscle
- Untangling the complexity of limb-girdle muscular dystrophies