Chorea-Acanthocytosis Genotype in the Original Critchley Kentucky Neuroacanthocytosis Kindred

OBJECTIVE: To determine the molecular nature of the neurological disease in the seminal family reported by Critchley et al in the 1960s, characterized by a hyperkinetic movement disorder and the appearance of acanthocytosis on peripheral blood smear. The eponym Levine-Critchley syndrome, subsequentl...

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Detalhes bibliográficos
Publicado no:Arch Neurol
Main Authors: Velayos-Baeza, Antonio, Holinski-Feder, Elke, Neitzel, Birgit, Bader, Benedikt, Critchley, Edmund M. R., Monaco, Anthony P., Danek, Adrian, Walker, Ruth H.
Formato: Artigo
Idioma:Inglês
Publicado em: 2011
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4615612/
https://ncbi.nlm.nih.gov/pubmed/21987550
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/archneurol.2011.239
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https://ncbi.nlm.nih.gov/pmc/articles/PMC4615612/
https://ncbi.nlm.nih.gov/pubmed/21987550
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/archneurol.2011.239

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