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Patients with a phenotype consistent with facioscapulohumeral muscular dystrophy display genetic and epigenetic heterogeneity.
scientific article published on 7 October 2011
Author/s
author: Sabrina Sacconi, Pilar Camaño, Adolfo López de Munain, Silvère M van der Maarel, Jessica C de Greef, Richard J L F Lemmers
Work details
Publication date
October 7, 2011
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Language
English
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