Abnormalities in the cerebral cortex in Gaucher disease type 1: Findings from the ENIGMA storage disease working group

被引：0
|
作者：
Karkashadze, George [1 ]
Namazova-Baranova, Leyla [1 ]
Belyaev, Mikhail [2 ]
Anikin, Anatoly [3 ]
Gundobina, Olga [3 ]
Vashakmadze, Nato [1 ]
Karkashadze, Magda [3 ]
Kapilushniy, Dmitry [3 ]
Gogberashvili, Tina [1 ]
Movsisyan, Goar [3 ]
Ermolina, Julia [3 ]
Konstsantinidi, Tatiana [1 ]
Solovieva, Anastasia [4 ]
Firumyants, Alexey [4 ]
Khrameeva, Ekaterina [2 ]
Gutman, Boris [5 ]
Zelman, Vladimir [5 ]
Thompson, Paul [5 ]
Baranov, Alexander [1 ]
机构：
[1] Sci Res Inst Pediat & Child Hlth CCH RAoS, Moscow, Russia
[2] Skolkovo Inst Sci & Technol, Moscow, Russia
[3] Natl Med Res Ctr Childrens Hlth MoH, Moscow, Russia
[4] Working Grp ENIGMA Storage Dis, Moscow, Russia
[5] Working Grp ENIGMA Storage Dis, Los Angeles, CA USA
来源：
MOLECULAR GENETICS AND METABOLISM | 2020年 / 129卷 / 02期
关键词：
D O I：
10.1016/j.ymgme.2019.11.206
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
197
引用
收藏
页码：S84 / S84
页数：1
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