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SELECTIVELY DIMINISHED CORPUS CALLOSUM FIBERS IN CONGENITAL CENTRAL HYPOVENTILATION SYNDROME
Congenital central hypoventilation syndrome (CCHS), a condition associated with mutations in the PHOX2B gene, is characterized by loss of breathing drive during sleep, insensitivity to CO(2) and O(2), and multiple somatomotor, autonomic, neuropsychological, and ophthalmologic deficits, including imp...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3048899/ https://ncbi.nlm.nih.gov/pubmed/21256194 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuroscience.2011.01.021 |
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