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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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| Publicado no: | BMC Neurol |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2015
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| Assuntos: | |
| Acesso em linha: | 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 |
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