Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by G. Deidda
Sequence Homology Between 4qter and 10qter Loci Facilitates the Instability of Subtelomeric KpnI Repeat Units Implicated in Facioscapulohumeral Muscular Dystrophy
American Journal of Human Genetics
Genetics
Related publications
Facioscapulohumeral Muscular Dystrophy
Rare Diseases
Facioscapulohumeral Muscular Dystrophy
Current Neurology and Neuroscience Reports
Neuroscience
Neurology
The Long and Short of Facioscapulohumeral Muscular Dystrophy
Electrical Impedance Myography in Facioscapulohumeral Muscular Dystrophy
Muscle and Nerve
Molecular Neuroscience
Neurology
Physiology
Cellular
Elderly Onset of Weakness in Facioscapulohumeral Muscular Dystrophy
Case Reports in Neurological Medicine
Facioscapulohumeral Muscular Dystrophy: Update on Pathogenesis and Future Treatments
Neurotherapeutics
Neurology
Pharmacology
Clinical and Genetic Features of Hearing Loss in Facioscapulohumeral Muscular Dystrophy
Neurology
Neurology
Three Novel Serum Biomarkers, miR-1, miR-133a, and miR-206 for Limb-Girdle Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, and Becker Muscular Dystrophy
Environmental Health and Preventive Medicine
Medicine
Environmental
Public Health
Occupational Health
Morpholino-Mediated Knockdown of DUX4 Toward Facioscapulohumeral Muscular Dystrophy Therapeutics
Molecular Therapy
Molecular Medicine
Molecular Biology
Pharmacology
Medicine
Genetics
Drug Discovery