APA (7th ed.) Citation

Douden, B. K. A., Abufara, Y. M. A., Aldrabeeh, M. F. A., Tell, N. R. M., & Abudaya, I. A rare case of adult-onset vanishing white matter leukoencephalopathy with movement disorder, expressing homozygous EIF2B3 and PRKN pathogenic variants. BMC.

Chicago Style (17th ed.) Citation

Douden, Bashar Kamal Ali, Yazan Mohammad Abdullah Abufara, Mahmood Fayez Ali Aldrabeeh, Naela Ramadan Mohammad Tell, and Ismail Abudaya. A Rare Case of Adult-onset Vanishing White Matter Leukoencephalopathy with Movement Disorder, Expressing Homozygous EIF2B3 and PRKN Pathogenic Variants. BMC.

MLA (9th ed.) Citation

Douden, Bashar Kamal Ali, et al. A Rare Case of Adult-onset Vanishing White Matter Leukoencephalopathy with Movement Disorder, Expressing Homozygous EIF2B3 and PRKN Pathogenic Variants. BMC.