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Publications by Rafaelle Bernard
Identification of Variants in the 4q35 GeneFAT1in Patients With a Facioscapulohumeral Dystrophy-Like Phenotype
Human Mutation
Genetics
Related publications
Identification of Variants in MBNL1 in Patients With a Myotonic Dystrophy-Like Phenotype
European Journal of Human Genetics
Genetics
Facioscapulohumeral Muscular Dystrophy
Rare Diseases
Facioscapulohumeral Muscular Dystrophy
Current Neurology and Neuroscience Reports
Neuroscience
Neurology
Thoracoscapular Fusion for Facioscapulohumeral Dystrophy
The Journal of Bone and Joint Surgery. British volume
Electrical Impedance Myography in Facioscapulohumeral Muscular Dystrophy
Muscle and Nerve
Molecular Neuroscience
Neurology
Physiology
Cellular
Distinguishing the 4qA and 4qB Variants Is Essential for the Diagnosis of Facioscapulohumeral Muscular Dystrophy in the Chinese Population
European Journal of Human Genetics
Genetics
The Long and Short of Facioscapulohumeral Muscular Dystrophy
Elderly Onset of Weakness in Facioscapulohumeral Muscular Dystrophy
Case Reports in Neurological Medicine
An RCS-Like Retinal Dystrophy Phenotype inMerKnockout Mice
Investigative Ophthalmology and Visual Science
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
