Citace podle APA

Dafsari, H. S., Kocaturk, N. M., Daimagüler, H., Brunn, A., Dötsch, J., Weis, J., . . . Cirak, S. (2019). Bi-allelic mutations in uncoordinated mutant number-45 myosin chaperone B are a cause for congenital myopathy. Acta Neuropathol Commun.

Styl Chicago

Dafsari, Hormos Salimi, Nur Mehpare Kocaturk, Hülya-Sevcan Daimagüler, Anna Brunn, Jörg Dötsch, Joachim Weis, Martina Deckert, a Sebahattin Cirak. "Bi-allelic Mutations in Uncoordinated Mutant Number-45 Myosin Chaperone B Are a Cause for Congenital Myopathy." Acta Neuropathol Commun 2019.

Citace podle MLA

Dafsari, Hormos Salimi, et al. "Bi-allelic Mutations in Uncoordinated Mutant Number-45 Myosin Chaperone B Are a Cause for Congenital Myopathy." Acta Neuropathol Commun 2019.

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