Congenital central hypoventilation syndrome, report of three cases

OBJECTIVE: To evaluate clinical characteristics and PHOX2B gene mutations in congenital central hypoventilation syndrome (CCHS) and to facilitate the early diagnosis and management of CCHS and reduce the misdiagnosis

Détails bibliographiques
Publié dans:Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 51(2013), 11 vom: 31. Nov., Seite 852-5
Auteur principal: Wang, Ying (Auteur)
Autres auteurs: He, Xi-yu, Yang, Yao, Chen, Xiao-chun
Format: Article
Langue:Chinese
Publié: 2013
Accès à la collection:Zhonghua er ke za zhi = Chinese journal of pediatrics
Sujets:Case Reports English Abstract Journal Article Homeodomain Proteins NBPhox protein Transcription Factors Carbon Dioxide 142M471B3J Alanine OF5P57N2ZX