Autosomal Recessive Spinocerebellar Ataxia Type 10: A Report of a New Case in Japan

Autosomal recessive spinocerebellar ataxia of type 10 (SCAR10) is a very rare neurodegenerative disease caused by mutations in the TMEM16K (ANO10) gene. This disorder is characterized by slowly progressive cerebellar ataxia and pyramidal signs inconstantly associated with cognitive decline, polyneur...

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Detalles Bibliográficos
Autores principales: Aida, Izumi, Ozawa, Tetsuo, Ohta, Kentaro, Fujinaka, Hidehiko, Goto, Kiyoe, Nakajima, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japanese Society of Internal Medicine 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449628/
https://www.ncbi.nlm.nih.gov/pubmed/35110481
http://dx.doi.org/10.2169/internalmedicine.8608-21

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449628/
https://www.ncbi.nlm.nih.gov/pubmed/35110481
http://dx.doi.org/10.2169/internalmedicine.8608-21

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