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families ataxia
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Curated Studies
Most Correlated Studies
OMIM - Multisystem Complex Disorders
OMIM - Congenital disorder
Mouse Phenotypes - Autosomal dominant hereditary disorder
OMIM - Epilepsy disorders
Friedreich’s ataxia induced pluripotent stem cells
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Literature
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Cerebellar cognitive-affective syndrome preceding ataxia associated with complex extrapyramidal feat…
MTSS1/Src family kinase dysregulation underlies multiple inherited ataxias.
A novel biallelic variant further delineates PRDX3-related autosomal recessive cerebellar ataxia.
DOCKopathies: A systematic review of the clinical pathologies associated with human DOCK pathogenic …
A novel KCNA1 mutation in a family with episodic ataxia and malignant hyperthermia.
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Transitional Life Events in Patients With Friedreich's Ataxia: Implications for Genetic Counseling
Transcranial Magnetic Stimulation in Spino-Cerebellar Ataxia
Sporadic Degenerative Ataxia With Adult Onset: Natural History Study
Coenzyme Q10 in Adult-Onset Ataxia
Investigating the Genetic and Phenotypic Presentation of Ataxia and Nucleotide Repeat Diseases
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