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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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| Udgivet i: | PLoS One |
|---|---|
| Main Authors: | , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Public Library of Science
2016
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| Fag: | |
| Online adgang: | 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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