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JMEDGENET-2011-100101
JMEDGENET-2011-100101
http://dx.doi.org/10.1136/JMEDGENET-2011-100101
Patients with a phenotype consistent with facioscapulohumeral muscular dystrophy display genetic and epigenetic heterogeneity.
P356
Q36576057-89B61732-7303-4E18-B8B7-03D163DCBC98
P356
JMEDGENET-2011-100101
http://dx.doi.org/10.1136/JMEDGENET-2011-100101