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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:PLoS One
Autors principals: Cobolli Gigli, Clementina, Scaramuzza, Linda, Gandaglia, Anna, Bellini, Elisa, Gabaglio, Marina, Parolaro, Daniela, Kilstrup-Nielsen, Charlotte, Landsberger, Nicoletta, Bedogni, Francesco
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2016
Matèries:
Research Article
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars