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Dysregulation of locus coeruleus development in congenital central hypoventilation syndrome
Human congenital central hypoventilation syndrome (CCHS), resulting from mutations in transcription factor PHOX2B, manifests with impaired responses to hypoxemia and hypercapnia especially during sleep. To identify brainstem structures developmentally affected in CCHS, we analyzed two postmortem neo...
Autores principales: | Nobuta, Hiroko, Cilio, Maria Roberta, Danhaive, Olivier, Tsai, Hui-Hsin, Tupal, Srinivasan, Chang, Sandra M., Murnen, Alice, Kreitzer, Faith, Bravo, Verenice, Czeisler, Catherine, Gokozan, Hamza Numan, Gygli, Patrick, Bush, Sean, Weese-Mayer, Debra E., Conklin, Bruce, Yee, Siu-Pok, Huang, Eric J., Gray, Paul A., Rowitch, David, Otero, José Javier |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4503865/ https://www.ncbi.nlm.nih.gov/pubmed/25975378 http://dx.doi.org/10.1007/s00401-015-1441-0 |
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