Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia

por Wakil, Salma M., Alhissi, Safa, Al Dossari, Haya, Alqahtani, Ayesha, Shibin, Sherin, Melaiki, Brahim T., Finsterer, Josef, Al-Hashem, Amal, Bohlega, Saeed, Alazami, Anas M.
Publicado 2019