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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...
Tallennettuna:
| Julkaisussa: | J Pediatr Neurosci |
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| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Medknow Publications & Media Pvt Ltd
2018
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| 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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