Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss (CAPOS): a new syndrome. - Abstract - Europe PMC
D-DEMØ, a distinct phenotype caused by ATP1A3 mutations | Neurology Genetics
NEURIMMINFL2014000778 1..3
Neuropatía auditiva en síndrome de capos pediátrico: Evolución favorable con implante coclear Auditory neuropathy in pediatr
A novel recurrent mutation in ATP1A3 causes CAPOS syndrome | Orphanet Journal of Rare Diseases | Full Text
Further characterization of CAPOS/CAOS syndrome with the Glu818Lys mutation in the ATP1A3 gene: A case report - ScienceDirect
PDF) A novel recurrent mutation in ATP1A3 causes CAPOS syndrome
Compilation of previously published diagnostic criteria for AHC, RDP,... | Download Table
What is ATP1A3 Gene CAPOS syndrome NGS Genetic DNA Test ?
CAPOS syndrome | Semantic Scholar
A new case of CAPOS/CAOS syndrome | Neurología (English Edition)
Desperate Parents Launch Campaign For Rare Disease Toddler Treatment ⋆ Madrid Metropolitan
Frontiers | Auditory Neuropathy as the Initial Phenotype for Patients With ATP1A3 c.2452 G > A: Genotype–Phenotype Study and CI Management
Frontiers | ATP1A3-Related Disorders: An Ever-Expanding Clinical Spectrum
Fever-related ataxia: a case report of CAPOS syndrome | Cerebellum & Ataxias | Full Text
Neuropatía auditiva en síndrome de capos pediátrico: Evolución favorable con implante coclear | Revista Portuguesa de Otorrinolaringologia e Cirurgia de Cabeça e Pescoço
RareConnect - 🔎We're looking for people affected by any of... | Facebook
Clinical features of 10 patients from three families with CAPOS syndrome | Download Table
Parents Battle For Cure For Toddler Plagued By Rare Disease - Zenger News
PDF) Fever-related ataxia: a case report of CAPOS syndrome
Fever-related ataxia: a case report of CAPOS syndrome | Cerebellum & Ataxias | Full Text
Cerebellar Ataxia, Areflexia, Pes Cavus, Optic Atrophy and Sensorineural Hearing Loss Syndrome
Parkinsonism & Related Disorders
Parents Battle For Cure For Toddler Plagued By Rare Disease - Zenger News
PDF) CAPOS syndrome and hemiplegic migraine in a novel pedigree with the specific ATP1A3 mutation
Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss (CAPOS): a new syndrome. - Abstract - Europe PMC
