APA

Elsayed L. E. O., Mohammed I. N., Hamed A. A. A., Elseed M. A., Salih M. A. M., Yahia A., Siddig R. A., Amin M., Koko M., Elbashir M. I., Ibrahim M. E., Brice A., Ahmed A. E. & Stevanin G. (20190225). Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family. : BMC medical genetics.

Chicago

Elsayed Liena E O, Mohammed Inaam N, Hamed Ahlam A A, Elseed Maha A, Salih Mustafa A M, Yahia Ashraf, Siddig Rayan A, Amin Mutaz, Koko Mahmoud, Elbashir Mustafa I, Ibrahim Muntaser E, Brice Alexis, Ahmed Ammar E and Stevanin Giovanni. 20190225. Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family. : BMC medical genetics.

Harvard

Elsayed L. E. O., Mohammed I. N., Hamed A. A. A., Elseed M. A., Salih M. A. M., Yahia A., Siddig R. A., Amin M., Koko M., Elbashir M. I., Ibrahim M. E., Brice A., Ahmed A. E. and Stevanin G. (20190225). Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family. : BMC medical genetics.

MLA

Elsayed Liena E O, Mohammed Inaam N, Hamed Ahlam A A, Elseed Maha A, Salih Mustafa A M, Yahia Ashraf, Siddig Rayan A, Amin Mutaz, Koko Mahmoud, Elbashir Mustafa I, Ibrahim Muntaser E, Brice Alexis, Ahmed Ammar E and Stevanin Giovanni. Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family. : BMC medical genetics. 20190225.