Biochemical and molecular-genetic analysis of two siblings with congenital disorder of glycosylation caused by a novel mutation in ATP6AP1 gene

被引：0
|
作者：
Ondruskova, Nina
Vondrackova, Alzbeta
Tesarova, Marketa
Honzik, Tomas
Zeman, Jiri
Hansikova, Hana
机构：
[1] Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague, Czech Republic
[2] Gen Univ Hosp, Prague, Czech Republic
来源：
GLYCOBIOLOGY | 2017年 / 27卷 / 12期
关键词：
D O I：
暂无
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：
118
引用
收藏
页码：1220 / 1220
页数：1
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