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Elsevier, Neuromuscular Disorders, 4-5(26), p. 300-308, 2016

DOI: 10.1016/j.nmd.2016.03.001

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Clinical, muscle pathological, and genetic features of Japanese facioscapulohumeral muscular dystrophy 2 (FSHD2) patients with SMCHD1 mutations

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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