Improving diagnosis of mitochondrial fatty-acid oxidation disorders

被引：4
|
作者：
Vianey-Saban, Christine [1 ]
Fouilhoux, Alain [2 ]
Vockley, Jerry [3 ]
Acquaviva-Bourdain, Cecile [1 ]
Guffon, Nathalie [2 ]
机构：
[1] CHU Lyon, Metab Inborn Errors Metab Unit, Biochem & Mol Biol Lab, Groupement Hosp Est, F-69500 Bron, France
[2] CHU Lyon, Natl Reference Ctr Hereditary Metab Dis, Groupement Hosp Est, F-69500 Bron, France
[3] Univ Pittsburgh, UPMC Childrens Hosp Pittsburgh, Ctr Rare Dis Therapy, Dept Pediat,Genet & Genom Med,Sch Med, Pittsburgh, PA 15224 USA
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2023年 / 31卷 / 03期
关键词：
D O I：
10.1038/s41431-022-01260-1
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
引用
收藏
页码：265 / 272
页数：8
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