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Genetic background of ataxia in children younger than 5 years in Finland

OBJECTIVE: To characterize the genetic background of molecularly undefined childhood-onset ataxias in Finland. METHODS: This study examined a cohort of patients from 50 families with onset of an ataxia syndrome before the age of 5 years collected from a single tertiary center, drawing on the advanta...

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Detalhes bibliográficos
Publicado no:Neurol Genet
Main Authors: Ignatius, Erika, Isohanni, Pirjo, Pohjanpelto, Max, Lahermo, Päivi, Ojanen, Simo, Brilhante, Virginia, Palin, Eino, Suomalainen, Anu, Lönnqvist, Tuula, Carroll, Christopher J.
Formato: Artigo
Idioma:Inglês
Publicado em: Wolters Kluwer 2020
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7323479/
https://ncbi.nlm.nih.gov/pubmed/32637629
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/NXG.0000000000000444
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