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Elsevier, Neuromuscular Disorders, 7(26), p. 472, 2016

DOI: 10.1016/j.nmd.2016.05.015

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Corrigendum to “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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