Author:
Nomura Shohei,Kashiwagi Mitsuru,Tanabe Takuya,Oba Chizu,Yanagi Kumiko,Kaname Tadashi,Okamoto Nobuhiko,Ashida Akira
Subject
Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health
Reference14 articles.
1. The expanding spectrum of neurological phenotypes in children with ATP1A3 mutations, alternating hemiplegia of childhood, rapid-onset dystonia-Parkinsonism, CAPOS and beyond;Sweney;Pediatr Neurol,2015
2. De novo mutations in ATP1A3 cause alternating hemiplegia of childhood;Heinzen;Nat Genet,2012
3. Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss (CAPOS): a new syndrome;Nicolaides;J Med Genet,1996
4. Relapsing encephalopathy with cerebellar ataxia related to an ATP1A3 mutation;Dard;Dev Med Child Neurol,2015
5. A case of early onset life-threatening epilepsy associated with a novel ATP1A3 gene variant;Ishihara;Brain Dev,2019
Cited by
3 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献