Dyfyniad APA

Dad, R., Walker, S., Scherer, S. W., Hassan, M. J., Alghamdi, M. D., Minassian, B. A., & Alkhater, R. A. (2017). Febrile ataxia and myokymia broaden the SPG26 hereditary spastic paraplegia phenotype. Neurol Genet.

Dyfyniad Arddull Chicago

Dad, Rubina, Susan Walker, Stephen W. Scherer, Muhammad Jawad Hassan, Mohammad Domaia Alghamdi, Berge A. Minassian, and Reem A. Alkhater. "Febrile Ataxia and Myokymia Broaden the SPG26 Hereditary Spastic Paraplegia Phenotype." Neurol Genet 2017.

Dyfyniad MLA

Dad, Rubina, et al. "Febrile Ataxia and Myokymia Broaden the SPG26 Hereditary Spastic Paraplegia Phenotype." Neurol Genet 2017.

Rhybudd: Mae'n bosib nad yw'r dyfyniadau hyn bob amser yn 100% cywir.