Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in Sudan

Elsayed, Liena E O and Mohammed, Inaam N and Hamed, Ahlam A A and Elseed, Maha A and Johnson, Adam and Mairey, Mathilde and Mohamed, Hassab Elrasoul S A and Idris, Mohamed N and Salih, Mustafa A M and El-sadig, Sarah M and Koko, Mahmoud E and Mohamed, Ashraf Y O and Raymond, Laure and Coutelier, Marie and Darios, Frédéric and Siddig, Rayan A and Ahmed, Ahmed K M A and Babai, Arwa M A and Malik, Hiba M O and Omer, Zulfa M B M and Mohamed, Eman O E and Eltahir, Hanan B and Magboul, Nasr Aldin A and Bushara, Elfatih E and Elnour, Abdelrahman and Rahim, Salah M Abdel and Alattaya, Abdelmoneim and Elbashir, Mustafa I and Ibrahim, Muntaser E and Durr, Alexandra and Audhya, Anjon and Brice, Alexis and Ahmed, Ammar E and Stevanin, Giovanni (2017) Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in Sudan. European Journal of Human Genetics, 25 (1). pp. 100-110. ISSN 1018-4813

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Item Type: Article
Subjects: R Medicine > RC Internal medicine > RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry
Depositing User: Moneeb Hassan
Date Deposited: 06 Jan 2018 20:12
Last Modified: 06 Jan 2018 20:12
URI: http://search.srh.edu.sd/id/eprint/2235

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