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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...
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. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
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 |
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