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Deep phenotyping of Facioscapulohumeral muscular dystrophy type 2 by magnetic resonance imaging
Download from api.wiley.comIntronic SMCHD1 variants in FSHD: testing the potential for CRISPR-Cas9 genome editing
UploadThe genetic basis of undiagnosed muscular dystrophies and myopathies
Download from www.ncbi.nlm.nih.govThe COQ2 genotype predicts the severity of Coenzyme Q10 deficiency
UploadCHCHD10mutations are not a common cause ofSMN1-negative type III/IV spinal motor atrophy
UploadConstruction of a Quality of Life Questionnaire for slowly progressive neuromuscular disease
Download from www.researchgate.netFacioscapulohumeral muscular dystrophy.
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