Identification of four novel mutations in VSP13A in Iranian patients with Chorea-acanthocytosis (ChAc) von Ghodsinezhad, Vadieh, Ghoreishi, Abdoreza, Rohani, Mohammad, Dadfar, Mahdi, Mohammadzadeh, Akbar, Rostami, Ali, Rahimi, Hamzeh

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P. Ala278Val mutation might cause a pathogenic defect in HEXB folding leading to the Sandhoff disease von Rahmani, Zahra, Banisadr, Arsham, Ghodsinezhad, Vadieh, Dibaj, Mohsen, Aryani, Omid

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