Publication | Closed Access
Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere
281
Citations
10
References
2002
Year
BiologyRare DiseasesFacioscapulohumeral Muscular DystrophyMendelian DisorderGenetic DisorderMedicineGeneticsDegenerative DiseaseMolecular GeneticsMedical GeneticsAnatomyNeuromuscular PathologyNeuromusculoskeletal Disorder
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