Cargando...
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...
Guardado en:
| Publicado en: | BMC Neurol |
|---|---|
| Autores principales: | , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
BioMed Central
2015
|
| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4391482/ https://ncbi.nlm.nih.gov/pubmed/25886294 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12883-015-0299-z |
| Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|