Cargando…
Collaborative Efforts for Spinocerebellar Ataxia Research in the United States: CRC-SCA and READISCA
Spinocerebellar ataxias are progressive neurodegenerative disorders primarily affecting the cerebellum. Although the first disease-causing gene was identified nearly 30 years ago, there is no known cure to date, and only a few options exist for symptomatic treatment, with modest effects. The recentl...
Autores principales: | Lin, Chih-Chun, Ashizawa, Tetsuo, Kuo, Sheng-Han |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7479060/ https://www.ncbi.nlm.nih.gov/pubmed/32982927 http://dx.doi.org/10.3389/fneur.2020.00902 |
Ejemplares similares
-
Inheritance patterns of ATCCT repeat interruptions in spinocerebellar ataxia type 10 (SCA10) expansions
por: Landrian, Ivette, et al.
Publicado: (2017) -
Spinocerebellar ataxia type 31 (SCA31)
por: Ishikawa, Kinya
Publicado: (2022) -
Expansion of the Spinocerebellar Ataxia Type 10 (SCA10) Repeat in a Patient with Sioux Native American Ancestry
por: Bushara, Khalaf, et al.
Publicado: (2013) -
Clinical and neuroradiological features of spinocerebellar ataxia 38 (SCA38)
por: Borroni, Barbara, et al.
Publicado: (2016) -
MME mutation in dominant spinocerebellar ataxia with neuropathy (SCA43)
por: Depondt, Chantal, et al.
Publicado: (2016)