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Deficient Purposeful Use of Forepaws in Female Mice Modelling Rett Syndrome
Rett syndrome (RTT) is a rare neurodevelopmental disorder, characterized by severe behavioural and physiological symptoms. Mutations in the methyl CpG binding protein 2 gene (MECP2) cause more than 95% of classic cases. Motor abnormalities represent a significant part of the spectrum of RTT symptoms...
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| Publicado no: | Neural Plast |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi Publishing Corporation
2015
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4491574/ https://ncbi.nlm.nih.gov/pubmed/26185689 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2015/326184 |
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