Oculomotor and visual axis systems sparing in spinocerebellar ataxia type 13R420H
dc.contributor.author | Waters, Michael F. | |
dc.contributor.author | Subramony, Sankarasubramoney H. | |
dc.contributor.author | Advincula, Joel | |
dc.contributor.author | Perlman, Susan | |
dc.contributor.author | Ashizawa, Tetsuo | |
dc.date.accessioned | 2024-04-27T01:41:48Z | |
dc.date.available | 2024-04-27T01:41:48Z | |
dc.date.issued | 2012-09-11 | |
dc.identifier.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. Neurology, 79(11), 1181-1182. https://doi.org/10.1212/WNL.0b013e3182698d5c | en |
dc.identifier.issn | 283-878 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14353/369 | |
dc.description.abstract | [No abstract available] | en |
dc.language.iso | en | en |
dc.publisher | Lippincott Williams and Wilkins | en |
dc.relation.uri | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3525304/ | en |
dc.subject | Nucleic acid binding protein | en |
dc.subject | Spinocerebellar ataxia type 13 protein | en |
dc.subject | Unclassified drug | en |
dc.subject | Voltage gated potassium channel | en |
dc.subject | KCNC3 protein, human | en |
dc.subject | Shaw potassium channel | en |
dc.subject | Allele | en |
dc.subject | Clinical protocol | en |
dc.subject | Dysarthria | en |
dc.subject | Epilepsy | en |
dc.subject | Filipino | en |
dc.subject | Gene mutation | en |
dc.subject | Genotype | en |
dc.subject | Human | en |
dc.subject | In vitro study | en |
dc.subject | Mental deficiency | en |
dc.subject | Note | en |
dc.subject | Oculomotor system | en |
dc.subject | Phenotype | en |
dc.subject | Priority journal | en |
dc.subject | Spinocerebellar ataxia type 13 | en |
dc.subject | Spinocerebellar degeneration | en |
dc.subject | Visual system | en |
dc.subject | Wild type | en |
dc.subject | Aged | en |
dc.subject | Article | en |
dc.subject | Child | en |
dc.subject | Eye movement | en |
dc.subject | Genetics | en |
dc.subject | Middle aged | en |
dc.subject | Phenotype | en |
dc.subject | Shaw Potassium Channels | en |
dc.subject.lcsh | Nucleic acids | en |
dc.subject.lcsh | Neurology | en |
dc.subject.lcsh | Research | en |
dc.subject.lcsh | Friedreich's ataxia | en |
dc.subject.lcsh | Medical protocols | en |
dc.subject.lcsh | Phenotype | en |
dc.subject.lcsh | Human genetics | en |
dc.subject.lcsh | Eye--Movements | en |
dc.subject.lcsh | Intellectual disability | en |
dc.subject.lcsh | Eye | en |
dc.subject.mesh | Spinocerebellar Degenerations | en |
dc.subject.mesh | Nucleic Acids | en |
dc.subject.mesh | Shaw Potassium Channels | en |
dc.subject.mesh | Phonetics | en |
dc.subject.mesh | Dysarthria | en |
dc.subject.mesh | Epilepsy | en |
dc.title | Oculomotor and visual axis systems sparing in spinocerebellar ataxia type 13R420H | en |
dc.type | Article | en |
dcterms.accessRights | Limited public access | en |
dc.citation.journaltitle | Neurology | en |
dc.citation.volume | 79 | en |
dc.citation.issue | 11 | en |
dc.citation.firstpage | 1181 | en |
dc.citation.lastpage | 1182 | en |
dc.identifier.doi | 10.1212/WNL.0b013e3182698d5c | |
local.isIndexedBy | ISI | en |
local.isIndexedBy | Scopus | en |
local.subject.agrovoc | nervous system diseases | en |
local.subject.agrovoc | nucleic acids | en |
local.subject.agrovoc | phenotypes | en |
local.subject.agrovoc | epilepsy | en |
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