A NOVEL CUTIS LAXA SYNDROME WITH CONGENITAL DISORDERS OF GLYCOSYLATION

被引：0
|
作者：
Morava, Eva [1 ]
Mohamed, Miski [2 ]
Gardeitchik, Thatjana [2 ]
Wevers, Ron [3 ]
机构：
[1] Tulane Univ, Sch Med, Hayward Genet Ctr, 1430 Tulane Ave, New Orleans, LA 70112 USA
[2] RadboudUMC Nijmegen, Dept Pediat, Nijmegen, Netherlands
[3] RadboudUMC Nijmegen, Dept Lab Sci, Nijmegen, Netherlands
来源：
MOLECULAR GENETICS AND METABOLISM | 2016年 / 117卷 / 03期
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D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
77
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收藏
页码：272 / 272
页数：1
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