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Merosin-deficient congenital muscular dystrophy, autosomal recessive (MDC1A, MIM#156225, LAMA2 gene coding for α2 chain of laminin)

Rare DiseasesDevelopmental BiologyMendelian DisorderGenetic DisorderMedicineGeneticsMolecular BiologyDegenerative Diseaseα2 ChainMolecular GeneticsDisease Gene IdentificationLama2 GeneNeuromuscular PathologyAutosomal Recessive