Glial scaffold required for cerebellar granule cell migration is dependent on dystroglycan function as a receptor for basement membrane proteins

BACKGROUND: Cobblestone lissencephaly is a severe neuronal migration disorder associated with congenital muscular dystrophies (CMD) such as Walker-Warburg syndrome, muscle-eye-brain disease, and Fukuyama-type CMD. In these severe forms of dystroglycanopathy, the muscular dystrophy and other tissue p...

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Autors principals: Nguyen, Huy, Ostendorf, Adam P, Satz, Jakob S, Westra, Steve, Ross-Barta, Susan E, Campbell, Kevin P, Moore, Steven A
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2013
Matèries:
Research
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3893534/
https://ncbi.nlm.nih.gov/pubmed/24252195
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2051-5960-1-58
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