Author:
Lin Yiming,Zheng Wenwei,Chen Yanru,Huang Chenggang,Fu Qingliu,Chen Dongmei,Peng Weilin
Funder
Huaqiao University
Fujian Provincial Health Technology Project
Quanzhou City Science and Technology Program
Natural Science Foundation of Fujian Province
Subject
Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine
Reference28 articles.
1. Glutaric acidemia type II: gene structure and mutations of the electron transfer flavoprotein:ubiquinone oxidoreductase (ETF:QO) gene;Goodman;Mol. Genet. Metab.,2002
2. Clinical and genetical heterogeneity of late-onset multiple acyl-coenzyme A dehydrogenase deficiency;Grunert;Orphanet J Rare Dis,2014
3. Division Of G, Metabolomics Child D, Health Care Branch Chinese Association For M, Child H, Chen X, Sun Y et al. [Consensus on screening, diagnosis and treatment of multiple acyl-CoA dehydrogenase deficiency]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2021, 38(5):414-418.
4. Prediction of disease severity in multiple acyl-CoA dehydrogenase deficiency: A retrospective and laboratory cohort study;van Rijt;J. Inherit. Metab. Dis.,2019
5. Multiple Acyl-CoA Dehydrogenase Deficiency with Variable Presentation Due to a Homozygous Mutation in a Bedouin Tribe;Staretz-Chacham;Genes (Basel),2021
Cited by
4 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献