APA

Mitsuhashi S., Boyden S. E., Estrella E. A., Jones T. I., Rahimov F., Yu T. W., Darras B. T., Amato A. A., Folkerth R. D., Jones P. L., Kunkel L. M. & Kang P. B. (20140724). Exome sequencing identifies a novel SMCHD1 mutation in facioscapulohumeral muscular dystrophy 2. : Neuromuscular disorders : NMD.

Chicago

Mitsuhashi Satomi, Boyden Steven E, Estrella Elicia A, Jones Takako I, Rahimov Fedik, Yu Timothy W, Darras Basil T, Amato Anthony A, Folkerth Rebecca D, Jones Peter L, Kunkel Louis M and Kang Peter B. 20140724. Exome sequencing identifies a novel SMCHD1 mutation in facioscapulohumeral muscular dystrophy 2. : Neuromuscular disorders : NMD.

Harvard

Mitsuhashi S., Boyden S. E., Estrella E. A., Jones T. I., Rahimov F., Yu T. W., Darras B. T., Amato A. A., Folkerth R. D., Jones P. L., Kunkel L. M. and Kang P. B. (20140724). Exome sequencing identifies a novel SMCHD1 mutation in facioscapulohumeral muscular dystrophy 2. : Neuromuscular disorders : NMD.

MLA

Mitsuhashi Satomi, Boyden Steven E, Estrella Elicia A, Jones Takako I, Rahimov Fedik, Yu Timothy W, Darras Basil T, Amato Anthony A, Folkerth Rebecca D, Jones Peter L, Kunkel Louis M and Kang Peter B. Exome sequencing identifies a novel SMCHD1 mutation in facioscapulohumeral muscular dystrophy 2. : Neuromuscular disorders : NMD. 20140724.