Gene expression signature of cerebellar hypoplasia in a mouse model of Down syndrome during postnatal development

BACKGROUND: Down syndrome is a chromosomal disorder caused by the presence of three copies of chromosome 21. The mechanisms by which this aneuploidy produces the complex and variable phenotype observed in people with Down syndrome are still under discussion. Recent studies have demonstrated an incre...

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Detalhes bibliográficos
Main Authors: Laffaire, Julien, Rivals, Isabelle, Dauphinot, Luce, Pasteau, Fabien, Wehrle, Rosine, Larrat, Benoit, Vitalis, Tania, Moldrich, Randal X, Rossier, Jean, Sinkus, Ralph, Herault, Yann, Dusart, Isabelle, Potier, Marie-Claude
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2009
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2678156/
https://ncbi.nlm.nih.gov/pubmed/19331679
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-10-138
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