Spinocerebellar Ataxia Type 6
What's New
Last Posted: Jan 04, 2025
- Apolipoprotein E epsilon4 allele is associated with better performance language and visual memory in spinocerebellar ataxia type 3.
Xuanyu Chen, et al. European journal of neurology 2024 0 (1) e70017 - Genetic Analysis of GCA Repeats in the GLS Gene: Implications for Undiagnosed Ataxia and Spinocerebellar Ataxia 3 in Mainland China.
Lijing Lei, et al. Movement disorders : official journal of the Movement Disorder Society 2024 0 - Regional distribution of polymorphisms associated to the disease-causing gene of spinocerebellar ataxia type 3.
Tim Lukas Elter, et al. Journal of neurology 2024 0 (1) 54 - Age-dependent somatic expansion of the ATXN3 CAG repeat in the blood and buccal swab DNA of individuals with spinocerebellar ataxia type 3/Machado-Joseph disease.
Ahmed M Sidky, et al. Human genetics 2024 0 - Spinocerebellar ataxia type 10 and Huntington disease-like 2 in Venezuela: Further evidence of two different ancestral founder effects.
Irene Paradisi, et al. Annals of human genetics 2024 0 - Spinocerebellar ataxia type 27B (SCA27B) in India: insights from a large cohort study suggest ancient origin.
Tiyasha De, et al. Neurogenetics 2024 0 - STUB1 Mutations as Possible Genetic Modifiers in Spinocerebellar Ataxia Type 8.
Raquel Baviera-Muñoz, et al. Movement disorders : official journal of the Movement Disorder Society 2024 0 - Spinocerebellar ataxia type 2 has multiple ancestral origins.
Lucas Schenatto Sena, et al. Parkinsonism & related disorders 2024 0 105985 - Repeat expansions in NOP56 are a cause of spinocerebellar ataxia Type 36 in the British population.
Tanya Lam, et al. Brain communications 2023 0 (5) fcad244 - Coexistence of multiple sclerosis and spinocerebellar ataxia type-8.
Nur Neyal, et al. Multiple sclerosis (Houndmills, Basingstoke, England) 2023 0 13524585231180549
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Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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