Upregulation of the Nr2f1-A830082K12Rik gene pair in murine neural crest cells results in a complex phenotype reminiscent of Waardenburg syndrome type 4

Waardenburg syndrome is a neurocristopathy characterized by a combination of skin and hair depigmentation, and inner ear defects. In the type 4 form, these defects show comorbidity with Hirschsprung disease, a disorder marked by an absence of neural ganglia in the distal colon, triggering functional...

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Detalles Bibliográficos
Autores principales: Bergeron, Karl-F., Nguyen, Chloé M. A., Cardinal, Tatiana, Charrier, Baptiste, Silversides, David W., Pilon, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2016
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117235/
https://www.ncbi.nlm.nih.gov/pubmed/27585883
http://dx.doi.org/10.1242/dmm.026773

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117235/
https://www.ncbi.nlm.nih.gov/pubmed/27585883
http://dx.doi.org/10.1242/dmm.026773

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