Oculomotor and visual axis systems sparing in spinocerebellar ataxia type 13R420H
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www.ncbi.nlm.nih.govDatum
2012-09-11Autor
MeSH term
Spinocerebellar Degenerations![MeSH MeSH](/themes/Mirage2/images/MeSH-logo.jpg)
Nucleic Acids
![MeSH MeSH](/themes/Mirage2/images/MeSH-logo.jpg)
Shaw Potassium Channels
![MeSH MeSH](/themes/Mirage2/images/MeSH-logo.jpg)
Phonetics
![MeSH MeSH](/themes/Mirage2/images/MeSH-logo.jpg)
Dysarthria
![MeSH MeSH](/themes/Mirage2/images/MeSH-logo.jpg)
Epilepsy
![MeSH MeSH](/themes/Mirage2/images/MeSH-logo.jpg)
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Zusammenfassung
[No abstract available]
Recommended Citation
Waters, M. F., Subramony, S. H., Advincula, J., Perlman, S., & Ashizawa, T. (2012). Oculomotor and visual axis systems sparing in spinocerebellar ataxia type 13R420H.Type
ArticleISSN
283-878Keywords
Nucleic acid binding protein Spinocerebellar ataxia type 13 protein Unclassified drug Voltage gated potassium channel KCNC3 protein, human Shaw potassium channel Allele Clinical protocol Dysarthria Epilepsy Filipino Gene mutation Genotype Human In vitro study Mental deficiency Note Oculomotor system Phenotype Priority journal Spinocerebellar ataxia type 13 Spinocerebellar degeneration Visual system Wild type Aged Article Child Eye movement Genetics Middle aged Phenotype Shaw Potassium Channels