Publication | Closed Access

Mutations in the laminin α2–chain gene (LAMA2) cause merosin–deficient congenital muscular dystrophy

Rare DiseasesLaminin α2–Chain GeneDevelopmental BiologyGenetic DisorderMedicineGeneticsMolecular BiologyDegenerative DiseaseMedical GeneticsDisease Gene IdentificationNeuromuscular Pathology