Analysis of autosomal dominant spinocerebellar ataxia type 1 in an extended family of central India

BACKGROUND: Spinocerebeller ataxia type 1 (SCA1) is a specific type of ataxia among a group of inherited diseases of the central nervous system. In SCA1, genetic defects lead to impairment of specific nerve fibers carrying messages to and from the brain, resulting in the degeneration of the cerebell...

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Detalles Bibliográficos
Autores principales: Sharma, Shashikant, Singh, Tekcham Dinesh, Poojary, Satish S., Rohilla, Manoj Singh, Singh, Ajaypal, Lowalekar, Kishore B., Tiwari, Pramod Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3656518/
https://www.ncbi.nlm.nih.gov/pubmed/23716937
http://dx.doi.org/10.4103/0971-6866.107981

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3656518/
https://www.ncbi.nlm.nih.gov/pubmed/23716937
http://dx.doi.org/10.4103/0971-6866.107981

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