Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations von Yahia, Ashraf, Hamed, Ahlam AA, Mohamed, Inaam N, Elseed, Maha A, Salih, Mustafa A, El-Sadig, Sarah M, Siddig, Hassab Elrasoul, Nasreldien, Ali Elsir Musa, Abdullah, Mohamed Ahmed, Elzubair, Maha, Omer, Farouk Yassen, Bakhiet, Aisha Motwakil, Abubaker, Rayan, Abozar, Fatima, Adil, Rawaa, Emad, Sara, Musallam, Mhammed Alhassan, Eltazi, Isra ZM, Omer, Zulfa, Malik, Hiba, Mohamed, Mayada OE, Elhassan, Ali A, Mohamed, Eman OE, Ahmed, Ahmed KMA, Ahmed, Elhami AA, Eltaraifee, Esraa, Hussein, Bidour K, Abd Allah, Amal SI, Salah, Lina, Nimir, Mohamed, Tag Elseed, Omnia M, Elhassan, Tasneem EA, Elbashier, Abubakr, Alfadul, Esraa SA, Fadul, Moneeb, Ali, Khalil F, Taha, Shaimaa Omer MA, Bushara, Elfatih E, Amin, Mutaz, Koko, Mahmoud, Ibrahim, Muntaser E, Ahmed, Ammar E, Elsayed, Liena EO, Stevanin, Giovanni

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