FKRP protein, human
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Skeletal muscle MRI of the lower limbs in congenital muscular dystrophy patients with novel <ce:italic>POMT1</ce:italic> and <ce:italic>POMT2</ce:italic> mutations
- Neuromuscular Disorders
Alpha-dystroglycanopathies form a genetically heterogeneous group of congenital muscular dystrophies with a large variety of… (More)
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