APA

Elsayed L. E. O., Mohammed I. N., Hamed A. A. A., Elseed M. A., Johnson A., Mairey M., Mohamed H. E. S. A., Idris M. N., Salih M. A. M., El-Sadig S. M., Koko M. E., Mohamed A. Y. O., Raymond L., Coutelier M., Darios F., Siddig R. A., Ahmed A. K. M. A., Babai A. M. A., Malik H. M. O., Omer Z. M. B. M., Mohamed E. O. E., Eltahir H. B., Magboul N. A. A., Bushara E. E., Elnour A., Rahim S. M. A., Alattaya A., Elbashir M. I., Ibrahim M. E., Durr A., Audhya A., Brice A., Ahmed A. E. & Stevanin G. (20170726). Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in Sudan. : European journal of human genetics : EJHG.

Chicago

Elsayed Liena E O, Mohammed Inaam N, Hamed Ahlam A A, Elseed Maha A, Johnson Adam, Mairey Mathilde, Mohamed Hassab Elrasoul S A, Idris Mohamed N, Salih Mustafa A M, El-Sadig Sarah M, Koko Mahmoud E, Mohamed Ashraf Y O, Raymond Laure, Coutelier Marie, Darios Frédéric, Siddig Rayan A, Ahmed Ahmed K M A, Babai Arwa M A, Malik Hiba M O, Omer Zulfa M B M, Mohamed Eman O E, Eltahir Hanan B, Magboul Nasr Aldin A, Bushara Elfatih E, Elnour Abdelrahman, Rahim Salah M Abdel, Alattaya Abdelmoneim, Elbashir Mustafa I, Ibrahim Muntaser E, Durr Alexandra, Audhya Anjon, Brice Alexis, Ahmed Ammar E and Stevanin Giovanni. 20170726. Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in Sudan. : European journal of human genetics : EJHG.

Harvard

Elsayed L. E. O., Mohammed I. N., Hamed A. A. A., Elseed M. A., Johnson A., Mairey M., Mohamed H. E. S. A., Idris M. N., Salih M. A. M., El-Sadig S. M., Koko M. E., Mohamed A. Y. O., Raymond L., Coutelier M., Darios F., Siddig R. A., Ahmed A. K. M. A., Babai A. M. A., Malik H. M. O., Omer Z. M. B. M., Mohamed E. O. E., Eltahir H. B., Magboul N. A. A., Bushara E. E., Elnour A., Rahim S. M. A., Alattaya A., Elbashir M. I., Ibrahim M. E., Durr A., Audhya A., Brice A., Ahmed A. E. and Stevanin G. (20170726). Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in Sudan. : European journal of human genetics : EJHG.

MLA

Elsayed Liena E O, Mohammed Inaam N, Hamed Ahlam A A, Elseed Maha A, Johnson Adam, Mairey Mathilde, Mohamed Hassab Elrasoul S A, Idris Mohamed N, Salih Mustafa A M, El-Sadig Sarah M, Koko Mahmoud E, Mohamed Ashraf Y O, Raymond Laure, Coutelier Marie, Darios Frédéric, Siddig Rayan A, Ahmed Ahmed K M A, Babai Arwa M A, Malik Hiba M O, Omer Zulfa M B M, Mohamed Eman O E, Eltahir Hanan B, Magboul Nasr Aldin A, Bushara Elfatih E, Elnour Abdelrahman, Rahim Salah M Abdel, Alattaya Abdelmoneim, Elbashir Mustafa I, Ibrahim Muntaser E, Durr Alexandra, Audhya Anjon, Brice Alexis, Ahmed Ammar E and Stevanin Giovanni. Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in Sudan. : European journal of human genetics : EJHG. 20170726.