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Myopathies without EOM Weakness: Facioscapulohumeral + Myotonic Dystrophy
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日期：2025-11-08
Myotonic dystrophy: Molecules & Signs Molecule change Related features Disease Mechanism DMPK reduction Muscle weakness Cardiac conduction Δ Na + channel defects Reduced Protein from mutated gene SIX5 reduction Cataracts Reduced Protein from...看更多
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