Neonatal apneic phenotype in a murine congenital central hypoventilation syndrome model is induced through non‐cell autonomous developmental mechanisms

Congenital central hypoventilation syndrome (CCHS) represents a rare genetic disorder usually caused by mutations in the homeodomain transcription factor PHOX2B. Some CCHS patients suffer mainly from deficiencies in CO(2) and/or O(2) respiratory chemoreflex, whereas other patients present with full...

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Detalles Bibliográficos
Autores principales: Alzate‐Correa, Diego, Mei‐ling Liu, Jillian, Jones, Mikayla, Silva, Talita M., Alves, Michele Joana, Burke, Elizabeth, Zuñiga, Jessica, Kaya, Behiye, Zaza, Giuliana, Aslan, Mehmet Tahir, Blackburn, Jessica, Shimada, Marina Y., Fernandes‐Junior, Silvio A., Baer, Lisa A., Stanford, Kristin I., Kempton, Amber, Smith, Sakima, Szujewski, Caroline C., Silbaugh, Abby, Viemari, Jean‐Charles, Takakura, Ana C., Garcia, Alfredo J., Moreira, Thiago S., Czeisler, Catherine M., Otero, José J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881415/
https://www.ncbi.nlm.nih.gov/pubmed/32654284
http://dx.doi.org/10.1111/bpa.12877

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881415/
https://www.ncbi.nlm.nih.gov/pubmed/32654284
http://dx.doi.org/10.1111/bpa.12877

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