Disease: Muscular dystrophy congenital- merosin negative
- A cryptic intronic LAMA2 insertion in a boy with mild congenital muscular dystrophy type 1A
- A difficult airway approach in a merosin-deficient congenital muscular dystrophy patient: a case report
- Clinical and genomic characteristics of LAMA2 related congenital muscular dystrophy in a patients' cohort from Qatar. A population specific founder variant
- Cobblestone Malformation in LAMA2 Congenital Muscular Dystrophy (MDC1A)
- Coexistence of Genetic Diseases Is a New Clinical Challenge: Three Unrelated Cases of Dual Diagnosis
- Exome sequencing detects compound heterozygous nonsense LAMA2 mutations in two siblings with atypical phenotype and nearly normal brain MRI
- Genetic blueprint of congenital muscular dystrophies with brain malformations in Egypt: A report of 11 families
- Genetics and muscle pathology in the diagnosis of muscular dystrophies: An update
- Identification of a compound heterozygous missense mutation in LAMA2 gene from a patient with merosin-deficient congenital muscular dystrophy type 1A
- Identification of a novel LAMA2 c.2217G > A, p.(Trp739*) mutation in a Moroccan patient with congenital muscular dystrophy: a case report
- Identification of a novel LAMA2 c.2217G > A, p.(Trp739*) mutation in a Moroccan patient with congenital muscular dystrophy: a case report
- Involvement of muscle satellite cell dysfunction in neuromuscular disorders: Expanding the portfolio of satellite cell-opathies
- Longitudinal changes in clinical outcome measures in COL6-related dystrophies and LAMA2-related dystrophies
- Lysosomes and the pathogenesis of merosin-deficient congenital muscular dystrophy
- Missense mutations in LAMA2 causing a new phenotype of mild cognitive impairment, proximal myopathy, seizure, and severe leukoencephalopathy: A case report and protein analysis
- Myelin abnormalities in merosin-deficient congenital muscular dystrophy
- Novel Homozygous Pathogenic Mutations of LAMA 2 Gene in Patients with Congen ital Muscular Dystrophy
- Rare variant in <em>LAMA2</em> gene causing congenital muscular dystrophy in a Sudanese family. A case report
- Whole exome sequencing identified a novel LAMA2 frameshift variant causing merosin-deficient congenital muscular dystrophy in a patient with cardiomyopathy, and autism-like behavior
- Whole-body muscle MRI characteristics of LAMA2-related congenital muscular dystrophy children: An emerging pattern
- Widening the spectrum of LAMA 2 congenital muscular dystrophy (MDC1A): cobblestone malformation