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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Detalles Bibliográficos
Autores principales: Incecik, Faruk, Herguner, Ozlem M., Willems, Patrick, Mungan, Neslihan O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909149/
https://www.ncbi.nlm.nih.gov/pubmed/29720801
http://dx.doi.org/10.4103/aian.AIAN_415_17

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909149/
https://www.ncbi.nlm.nih.gov/pubmed/29720801
http://dx.doi.org/10.4103/aian.AIAN_415_17

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