Mitsuhashi, S., Boyden, S. E., Estrella, E. A., Jones, T. I., Rahimov, F., Yu, T. W., . . . Kang, P. B. (2013). Exome sequencing identifies a novel SMCHD1 mutation in facioscapulohumeral muscular dystrophy 2.
Citação norma ChicagoMitsuhashi, Satomi, et al. Exome Sequencing Identifies a Novel SMCHD1 Mutation in Facioscapulohumeral Muscular Dystrophy 2. 2013.
MLA CitationMitsuhashi, Satomi, et al. Exome Sequencing Identifies a Novel SMCHD1 Mutation in Facioscapulohumeral Muscular Dystrophy 2. 2013.
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