Research Advances on Therapeutic Approaches to Congenital Central Hypoventilation Syndrome (CCHS)

Congenital central hypoventilation syndrome (CCHS) is a genetic disorder of neurodevelopment, with an autosomal dominant transmission, caused by heterozygous mutations in the PHOX2B gene. CCHS is a rare disorder characterized by hypoventilation due to the failure of autonomic control of breathing. U...

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Detalles Bibliográficos
Autores principales: Di Lascio, Simona, Benfante, Roberta, Cardani, Silvia, Fornasari, Diego
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7835644/
https://www.ncbi.nlm.nih.gov/pubmed/33510615
http://dx.doi.org/10.3389/fnins.2020.615666

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7835644/
https://www.ncbi.nlm.nih.gov/pubmed/33510615
http://dx.doi.org/10.3389/fnins.2020.615666

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