Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations.
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G. Stevanin | A. Bakhiet | M. Ibrahim | M. Abdullah | M. Salih | M. Koko | L. Elsayed | A. Hamed | A. Ahmed | H. E. Siddig | I. Mohamed | S. El-sadig | R. Abubaker | Esraa Eltaraifee | Ashraf Yahia | Amal S. I. Abd Allah | Maha A. Elseed | Farouk Yassen Omer | Fatima Abozar | Rawaa Adil | Sara Emad | Mhammed Alhassan Musallam | I. Eltazi | Elhami A. A. Ahmed | Khalil Ali | M. Amin | Eman O E Mohamed | Bidour K. Hussein | Ahmed A Ahmed | Zulfa Omer | Moneeb Fadul | A. Nasreldien | Maha Elzubair | Hiba Malik | Mayada O E Mohamed | Ali A. Elhassan | Lina Salah | Mohamed Nimir | Omnia M Tag Elseed | Tasneem E A Elhassan | Abubakr Elbashier | Esraa S A Alfadul | S. Taha | Elfatih E Bushara | S. El-Sadig