Molecular epidemiology of hereditary ataxia in Finland

BACKGROUND: The genetics of cerebellar ataxia is complex. Hundreds of causative genes have been identified, but only a few cause more than single cases. The spectrum of ataxia-causing genes differs considerably between populations. The aim of the study was to investigate the molecular epidemiology o...

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Detalles Bibliográficos
Autores principales: Lipponen, Joonas, Helisalmi, Seppo, Raivo, Joose, Siitonen, Ari, Doi, Hiroshi, Rusanen, Harri, Lehtilahti, Maria, Ryytty, Mervi, Laakso, Markku, Tanaka, Fumiaki, Majamaa, Kari, Kytövuori, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487109/
https://www.ncbi.nlm.nih.gov/pubmed/34600502
http://dx.doi.org/10.1186/s12883-021-02409-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487109/
https://www.ncbi.nlm.nih.gov/pubmed/34600502
http://dx.doi.org/10.1186/s12883-021-02409-z

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