Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Paraplegia and ATP13A2[original query] |
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Clinical exome sequencing for cerebellar ataxia and spastic paraplegia uncovers novel gene-disease associations and unanticipated rare disorders. European journal of human genetics : EJHG 2016 May . van de Warrenburg Bart P, Schouten Meyke I, de Bot Susanne T, Vermeer Sascha, Meijer Rowdy, Pennings Maartje, Gilissen Christian, Willemsen Michèl Aap, Scheffer Hans, Kamsteeg Erik-J |
Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegia. Translational neurodegeneration 2019 8 19. Wei Qiao, Dong Hai-Lin, Pan Li-Ying, Chen Cong-Xin, Yan Yang-Tian, Wang Rou-Min, Li Hong-Fu, Liu Zhi-Jun, Tao Qing-Qing, Wu Zhi-Yi |
Autosomal Recessive Spastic Paraplegia Type 78 Associated with a Homozygous Variant in the ATP13A2 Gene. Movement disorders clinical practice 2022 10 9 (7): 997-1002. Algahtani Hussein, Shirah Bader, Alshammari Salem, Alghamdi Fareeda, Abdulkareem Angham Abdulrhman, Naseer Muhammad Imr |
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- Page last updated:Apr 16, 2024
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