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Autosomal-Recessive Spastic Ataxia of Charlevoix-Saguenay: A Turkish Child

Autosomal-recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is caused by mutations of the SACS gene, characterized by late-infantile-onset spastic ataxia and other neurological features. ARSACS has a high prevalence in northeastern Quebec, Canada. Recently, several ARSACS cases have been repo...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:J Pediatr Neurosci
Päätekijät: Incecik, Faruk, Hergüner, Ozlem M., Bisgin, Atil
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Medknow Publications & Media Pvt Ltd 2018
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC6144602/
https://ncbi.nlm.nih.gov/pubmed/30271475
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/JPN.JPN_8_18
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