tailieunhanh - Compound heterozygous POMGNT1 mutations leading to muscular dystrophydystroglycanopathy type A3: A case report

Dystroglycanopathies, which are caused by reduced glycosylation of alpha-dystroglycan, are a heterogeneous group of neurodegenerative disorders characterized by variable brain and skeletal muscle involvement. | Compound heterozygous POMGNT1 mutations leading to muscular dystrophydystroglycanopathy type A3: A case report

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