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	1.	Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family. [electronic resource] by 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 Stevanin, Giovanni Producer: 20190225 In: BMC medical genetics vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in Sudan. [electronic resource] by 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 Stevanin, Giovanni Producer: 20170726 In: European journal of human genetics : EJHG vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)