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

    Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia by Salma M. Wakil, Safa Alhissi, Haya Al Dossari, Ayesha Alqahtani, Sherin Shibin, Brahim T. Melaiki, Josef Finsterer, Amal Al-Hashem, Saeed Bohlega, Anas M. Alazami

    Published 2019-07-01
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