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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Détails bibliographiques
| Publié dans: | Neural plasticity. - 1998. - 2015(2015) vom: 10., Seite 326184
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| Auteur principal: |
De Filippis, Bianca
(Auteur) |
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| Autres auteurs: |
Musto, Mattia,
Altabella, Luisa,
Romano, Emilia,
Canese, Rossella,
Laviola, Giovanni |
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| Format: | Article en ligne
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| Langue: | English |
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| Publié: |
2015
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| Accès à la collection: | Neural plasticity
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| Sujets: | Journal Article
Research Support, Non-U.S. Gov't
Mecp2 protein, mouse
Methyl-CpG-Binding Protein 2 |
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