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Mutations In Rare Ataxia Genes Are Uncommon Causes of Sporadic Cerebellar Ataxia

BACKGROUND: Sporadic-onset ataxia is common in a tertiary care setting but a significant percentage remains unidentified despite extensive evaluation. Rare genetic ataxias, reported only in specific populations or families, may contribute to a percentage of sporadic ataxia. METHODS: Patients with ad...

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Bibliografski detalji
Glavni autori: Fogel, Brent L., Lee, Ji Yong, Lane, Jessica, Wahnich, Amanda, Chan, Sandy, Huang, Alden, Osborn, Greg E., Klein, Eric, Mamah, Catherine, Perlman, Susan, Geschwind, Daniel H., Coppola, Giovanni
Format: Artigo
Jezik:Inglês
Izdano: 2012
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3323119/
https://ncbi.nlm.nih.gov/pubmed/22287014
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mds.24064
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