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Neurocognition in Congenital Central Hypoventilation Syndrome: influence of genotype and ventilation method

BACKGROUND: Congenital Central Hypoventilation Syndrome (CCHS) is characterized by central hypoventilation due to abnormal autonomic control of breathing and global dysautonomia. Patients harbour heterozygous PHOX-2B gene mutations which are polyalanine repeats of various lengths in most of the case...

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Detalles Bibliográficos
Autores principales:	Trang, Ha, Bourgeois, Pauline, Cheliout-Heraut, Fawzia
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2020
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7670788/ https://www.ncbi.nlm.nih.gov/pubmed/33203435 http://dx.doi.org/10.1186/s13023-020-01601-7

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