Parkinsonism & Related Disorders
Further characterization of CAPOS/CAOS syndrome with the Glu818Lys mutation in the ATP1A3 gene: A case report | Semantic Scholar
The Genetic Homogeneity of CAPOS Syndrome: Four New Patients With the c.2452G>A (p.Glu818Lys) Mutation in the ATP1A3 Gene
Chronological dynamic changes in cortico-subcortical imbalance of cerebral blood flow in a boy with CAPOS syndrome - ScienceDirect
RareConnect - 🔎We're looking for people affected by any of... | Facebook
Parents Battle For Cure For Toddler Plagued By Rare Disease - Zenger News
Clinical features of 10 patients from three families with CAPOS syndrome | Download Table
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss (CAPOS): a new syndrome. - Abstract - Europe PMC
Desperate Parents Launch Campaign For Rare Disease Toddler Treatment ⋆ Madrid Metropolitan
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss (CAPOS): a new syndrome. - Abstract - Europe PMC
Parkinsonism & Related Disorders on Twitter: "#Dystonia #deafness #ATP1A3 # CAPOS Log in to: https://t.co/OaOj1URbYq https://t.co/xQ0wsK7k1g" / Twitter
Genes | Free Full-Text | Review of Ocular Manifestations of Joubert Syndrome
Compilation of previously published diagnostic criteria for AHC, RDP,... | Download Table
A new case of CAPOS/CAOS syndrome
A novel recurrent mutation in ATP1A3 causes CAPOS syndrome | Orphanet Journal of Rare Diseases | Full Text
NEURIMMINFL2014000778 1..3
Fever-related ataxia: a case report of CAPOS syndrome | Cerebellum & Ataxias | Full Text
CAPOS syndrome | Semantic Scholar
De novo ATP1A3 variants cause polymicrogyria | Science Advances
What is ATP1A3 Gene CAPOS syndrome NGS Genetic DNA Test ?
ATP1A3 spectrum disorders: A video-documented history of 7 genetically confirmed early onset cases - ScienceDirect
Parents Battle For Cure For Toddler Plagued By Rare Disease - Zenger News
