Childhood‐Onset Choreo‐Dystonia Due to a Recurrent Novel Homozygous Nonsense <scp><i>HPCA</i></scp> Variant: Case Series and Literature Review
Francesca Magrinelli(National Hospital for Neurology and Neurosurgery), Reza Maroofian(National Hospital for Neurology and Neurosurgery), Fatemeh Arab(Tehran University of Medical Sciences), Maedeh Neshatdoust(Isfahan University of Technology), Clarissa Rocca(Institute of Human Genetics), Behnaz Ansari(Isfahan University of Medical Sciences), Ehsan Ghayoor Karimiani(St George's, University of London), Henry Houlden(University College London), Sahar Sedighzadeh(Shahid Chamran University of Ahvaz), Kailash P. Bhatia(National Hospital for Neurology and Neurosurgery), Mehran Beiraghi Toosi(Mashhad University of Medical Sciences)
Cited by 7
Related Papers
Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria
|Movement Disorders|2017|2.3k
Genome-wide association study reveals genetic risk underlying Parkinson's disease
|Nature Genetics|2009|2k
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease
|Proceedings of the National Academy of Sciences|2014|367