Abnormal auditory pathways in PHOX2B mutation positive congenital central hypoventilation syndrome

BACKGROUND: Congenital central hypoventilation syndrome (CCHS) is a rare disease characterized by severe central hypoventilation due to abnormal autonomic control of breathing. The PHOX2B gene, mutations of which define the disease, is expressed in a group of nuclei located in brainstem areas. Pathw...

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Detalles Bibliográficos
Autores principales: Trang, Ha, Masri Zada, Tarif, Heraut, Fawzia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4391482/
https://www.ncbi.nlm.nih.gov/pubmed/25886294
http://dx.doi.org/10.1186/s12883-015-0299-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4391482/
https://www.ncbi.nlm.nih.gov/pubmed/25886294
http://dx.doi.org/10.1186/s12883-015-0299-z

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