Huntingtine et mitose
La maladie de Huntington (MH) est une maladie neurodégénérative héréditaire autosomique dominante. Elle résulte d’une expansion anormale de glutamines (polyQ) dans la partie N-terminale de la protéine huntingtine (HTT ; codé par HTT). La MH est caractérisée par la dysfonction et la mort de cellules...
Main Author: | Molina-Calavita, Maria |
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Other Authors: | Paris 11 |
Language: | en |
Published: |
2012
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Subjects: | |
Online Access: | http://www.theses.fr/2012PA114845/document |
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