Neuronal ceroid lipofuscinoses type 8: Expanding genotype/phenotype diversity-first report from Saudi Arabia von Alkhars, Fatimah Z, Bo Ali, Ahmed Y, Almohanna, Mostafa A, Almajhad, Nabil A

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Neurological expression of an inherited translocation of chromosomal 1 and 7 von AlMajhad, Nabil A, AlHashem, Amal M, Bouhjar, Inesse A, Tabarki, Brahim M

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Homozygous KCNMA1 mutation as a cause of cerebellar atrophy, developmental delay and seizures von Tabarki, Brahim, AlMajhad, Nabil, AlHashem, Amal, Shaheen, Ranad, Alkuraya, Fowzan S.

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Spinal Muscular Atrophy and Communicating Hydrocephalus: A Novel or a Well-Established Rare Association? von Alkhars, Fatimah Z, Almajhad, Nabil, Al-Obaid, Jaafer, Alghadeer, Fatimah, Bo Ali, Ahmed Y

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Spinal Muscular Atrophy and Communicating Hydrocephalus: A Novel or a Well-Established Rare Association? von Alkhars, Fatimah Z, Almajhad, Nabil, Al-Obaid, Jaafer, Alghadeer, Fatimah, Bo Ali, Ahmed Y

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