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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:PLoS One
Päätekijät: Cobolli Gigli, Clementina, Scaramuzza, Linda, Gandaglia, Anna, Bellini, Elisa, Gabaglio, Marina, Parolaro, Daniela, Kilstrup-Nielsen, Charlotte, Landsberger, Nicoletta, Bedogni, Francesco
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Public Library of Science 2016
Aiheet:
Research Article
Linkit: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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