MeCP2 Related Studies Benefit from the Use of CD1 as Genetic Background

MECP2 mutations cause a number of neurological disorders of which Rett syndrome (RTT) represents the most thoroughly analysed condition. Many Mecp2 mouse models have been generated through the years; their validity is demonstrated by the presence of a broad spectrum of phenotypes largely mimicking t...

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Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: Cobolli Gigli, Clementina, Scaramuzza, Linda, Gandaglia, Anna, Bellini, Elisa, Gabaglio, Marina, Parolaro, Daniela, Kilstrup-Nielsen, Charlotte, Landsberger, Nicoletta, Bedogni, Francesco
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2016
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4838291/
https://ncbi.nlm.nih.gov/pubmed/27097329
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0153473
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