COL4A1 Mutations Cause Ocular Dysgenesis, Neuronal Localization Defects, and Myopathy in Mice and Walker-Warburg Syndrome in Humans

Muscle-eye-brain disease (MEB) and Walker Warburg Syndrome (WWS) belong to a spectrum of autosomal recessive diseases characterized by ocular dysgenesis, neuronal migration defects, and congenital muscular dystrophy. Until now, the pathophysiology of MEB/WWS has been attributed to alteration in dyst...

Descripción completa

Detalles Bibliográficos
Autores principales: Labelle-Dumais, Cassandre, Dilworth, David J., Harrington, Emily P., de Leau, Michelle, Lyons, David, Kabaeva, Zhyldyz, Manzini, M. Chiara, Dobyns, William B., Walsh, Christopher A., Michele, Daniel E., Gould, Douglas B.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3098190/
https://www.ncbi.nlm.nih.gov/pubmed/21625620
http://dx.doi.org/10.1371/journal.pgen.1002062

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3098190/
https://www.ncbi.nlm.nih.gov/pubmed/21625620
http://dx.doi.org/10.1371/journal.pgen.1002062

Ejemplares similares