Loss of Ikbkap Causes Slow, Progressive Retinal Degeneration in a Mouse Model of Familial Dysautonomia

Familial dysautonomia (FD) is an autosomal recessive congenital neuropathy that is caused by a mutation in the gene for inhibitor of kappa B kinase complex-associated protein (IKBKAP). Although FD patients suffer from multiple neuropathies, a major debilitation that affects their quality of life is...

Descripción completa

Detalles Bibliográficos
Autores principales: Ueki, Yumi, Ramirez, Grisela, Salcedo, Ernesto, Stabio, Maureen E., Lefcort, Frances
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2016
Materias:
New Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037323/
https://www.ncbi.nlm.nih.gov/pubmed/27699209
http://dx.doi.org/10.1523/ENEURO.0143-16.2016

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037323/
https://www.ncbi.nlm.nih.gov/pubmed/27699209
http://dx.doi.org/10.1523/ENEURO.0143-16.2016

Ejemplares similares