Defective exercise-related expiratory muscle recruitment in patients with PHOX2B mutations: A clue to neural determinants of the congenital central hypoventilation syndrome.

已完结 10 由 liu 发布于 2025/4/12 22:27:32

DOI:10.1016/j.pulmoe.2024.01.005
作者：P Laveneziana,?Q Fossé,?M Bret,?M Patout,?B Dudoignon,?C Llontop,?C Morélot-Panzini,?F Cayetanot,?L Bodineau,?C Straus,?T Similowski
文献类型：期刊论文
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Taylor & Francis

Abstract：Introduction and objectives: The human congenital central hypoventilation syndrome (CCHS) is caused by mutations in the PHOX2B (paired-like homeobox 2B) gene. Genetically engineered PHOX2B r

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