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Spinocerebellar Ataxia-21 in a Turkish Child

Hereditary cerebellar ataxias are genetically heterogeneous disorders. Autosomal recessive spinocerebellar ataxia-21 (SCAR21) is a neurologic disorder characterized by the onset of cerebellar ataxia, recurrent episodes of liver failure, peripheral neuropathy, and learning disabilities. Herein, we re...

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Dades bibliogràfiques
Publicat a:Ann Indian Acad Neurol
Autors principals: Incecik, Faruk, Herguner, Ozlem M., Willems, Patrick, Mungan, Neslihan O.
Format: Artigo
Idioma:Inglês
Publicat: Medknow Publications & Media Pvt Ltd 2018
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5909149/
https://ncbi.nlm.nih.gov/pubmed/29720801
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/aian.AIAN_415_17
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