EYA1 mutations associated with the branchio-oto-renal syndrome result in defective otic development in Xenopus laevis

Background information. The BOR (branchio-oto-renal) syndrome is a dominant disorder most commonly caused by mutations in the EYA1 (Eyes Absent 1) gene. Symptoms commonly include deafness and renal anomalies. Results. We have used the embryos of the frog Xenopus laevis as an animal model for early e...

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Detalles Bibliográficos
Autores principales: Li, Youe, Manaligod, Jose M., Weeks, Daniel L.
Formato: Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2825735/
https://www.ncbi.nlm.nih.gov/pubmed/19951260
http://dx.doi.org/10.1042/BC20090098

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2825735/
https://www.ncbi.nlm.nih.gov/pubmed/19951260
http://dx.doi.org/10.1042/BC20090098

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