Molecular epidemiology of hereditary ataxia in Finland

Molecular epidemiology of hereditary ataxia in Finland

Abstract 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 epidem...

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Bibliographic Details
Main Authors: Joonas Lipponen, Seppo Helisalmi, Joose Raivo, Ari Siitonen, Hiroshi Doi, Harri Rusanen, Maria Lehtilahti, Mervi Ryytty, Markku Laakso, Fumiaki Tanaka, Kari Majamaa, Laura Kytövuori
Format: Article
Language:English
Published: BMC 2021-10-01
Series:BMC Neurology
Subjects:
CANVAS
Hereditary ataxia
Molecular epidemiology
Repeat expansion
Online Access:https://doi.org/10.1186/s12883-021-02409-z

Internet

https://doi.org/10.1186/s12883-021-02409-z

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