Carregant...
A mutation in the Tubb4a gene leads to microtubule accumulation with hypomyelination and demyelination
OBJECTIVE: Our goal was to define the genetic cause of the profound hypomyelination in the taiep rat model and determine its relevance to human white matter disease. METHODS: Based on previous localization of the taiep mutation to rat chromosome 9, we tested if the mutation resided within the Tubb4a...
Guardat en:
| Publicat a: | Ann Neurol |
|---|---|
| Autors principals: | , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2017
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5495199/ https://ncbi.nlm.nih.gov/pubmed/28393430 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ana.24930 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|