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Erythrocytes (RBCs) (1)
Facioscapulohumeral muscular dystrophy (1)
Familial adult myoclonic epilepsy (FAME) (1)
Familial Cortical Myoclonic Tremor with Epilepsy (FCMTE) (1)
Female patients (1)
Fibrin network (1)
Fibrin networks (1)
G2019S mutation (1)
Gastrointestinal tract (1)
GBA variants (1)
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