A family with two children diagnosed with aspartylglucosaminuria-case report and literature review

OBJECTIVE: The authors sought to investigate the clinical features and characteristics of genetic mutation in patients with aspartylglucosaminuria

Détails bibliographiques
Publié dans:Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 52(2014), 6 vom: 04. Juni, Seite 455-9
Auteur principal: Liu, Yujie (Auteur)
Autres auteurs: Zou, Liping, Meng, Yan, Zhang, Ying, Shi, Xiuyu, Ju, Jun, Yang, Guang, Hu, Linyan, Chen, Xiaoqiao
Format: Article
Langue:Chinese
Publié: 2014
Accès à la collection:Zhonghua er ke za zhi = Chinese journal of pediatrics
Sujets:Case Reports English Abstract Journal Article Review Biomarkers Aspartylglucosylaminase EC 3.5.1.26