APA
Donkervoort S., Sabouny R., Yun P., Gauquelin L., Chao K. R., Hu Y., Al Khatib I., Töpf A., Mohassel P., Cummings B. B., Kaur R., Saade D., Moore S. A., Waddell L. B., Farrar M. A., Goodrich J. K., Uapinyoying P., Chan S. H. S., Javed A., Leach M. E., Karachunski P., Dalton J., Medne L., Harper A., Thompson C., Thiffault I., Specht S., Lamont R. E., Saunders C., Racher H., Bernier F. P., Mowat D., Witting N., Vissing J., Hanson R., Coffman K. A., Hainlen M., Parboosingh J. S., Carnevale A., Yoon G., Schnur R. E., Boycott K. M., Mah J. K., Straub V., Foley A. R., Innes A. M., Bönnemann C. G. & Shutt T. E. (20200903). MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement. : Acta neuropathologica.
Chicago
Donkervoort S, Sabouny R, Yun P, Gauquelin L, Chao K R, Hu Y, Al Khatib I, Töpf A, Mohassel P, Cummings B B, Kaur R, Saade D, Moore S A, Waddell L B, Farrar M A, Goodrich J K, Uapinyoying P, Chan S H S, Javed A, Leach M E, Karachunski P, Dalton J, Medne L, Harper A, Thompson C, Thiffault I, Specht S, Lamont R E, Saunders C, Racher H, Bernier F P, Mowat D, Witting N, Vissing J, Hanson R, Coffman K A, Hainlen M, Parboosingh J S, Carnevale A, Yoon G, Schnur R E, Boycott K M, Mah J K, Straub V, Foley A Reghan, Innes A M, Bönnemann C G and Shutt T E. 20200903. MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement. : Acta neuropathologica.
Harvard
Donkervoort S., Sabouny R., Yun P., Gauquelin L., Chao K. R., Hu Y., Al Khatib I., Töpf A., Mohassel P., Cummings B. B., Kaur R., Saade D., Moore S. A., Waddell L. B., Farrar M. A., Goodrich J. K., Uapinyoying P., Chan S. H. S., Javed A., Leach M. E., Karachunski P., Dalton J., Medne L., Harper A., Thompson C., Thiffault I., Specht S., Lamont R. E., Saunders C., Racher H., Bernier F. P., Mowat D., Witting N., Vissing J., Hanson R., Coffman K. A., Hainlen M., Parboosingh J. S., Carnevale A., Yoon G., Schnur R. E., Boycott K. M., Mah J. K., Straub V., Foley A. R., Innes A. M., Bönnemann C. G. and Shutt T. E. (20200903). MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement. : Acta neuropathologica.
MLA
Donkervoort S, Sabouny R, Yun P, Gauquelin L, Chao K R, Hu Y, Al Khatib I, Töpf A, Mohassel P, Cummings B B, Kaur R, Saade D, Moore S A, Waddell L B, Farrar M A, Goodrich J K, Uapinyoying P, Chan S H S, Javed A, Leach M E, Karachunski P, Dalton J, Medne L, Harper A, Thompson C, Thiffault I, Specht S, Lamont R E, Saunders C, Racher H, Bernier F P, Mowat D, Witting N, Vissing J, Hanson R, Coffman K A, Hainlen M, Parboosingh J S, Carnevale A, Yoon G, Schnur R E, Boycott K M, Mah J K, Straub V, Foley A Reghan, Innes A M, Bönnemann C G and Shutt T E. MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement. : Acta neuropathologica. 20200903.