Response: Late-onset Pompe disease manifests in the brain

被引：2
|
作者：
Schneider, Ilka [1 ]
Hensel, Ole [1 ]
Zierz, Stephan [1 ]
机构：
[1] Martin Luther Univ Halle Saale, Dept Neurol, Ernst Grube Str 40, D-06120 Halle, Saale, Germany
来源：
MOLECULAR GENETICS AND METABOLISM REPORTS | 2019年 / 21卷
关键词：
Late onset Pompe disease (LOPD); White matter lesions; Fazekas grade; alpha-1,4 glucosidase; Enzyme replacement therapy (ERT);
D O I：
10.1016/j.ymgmr.2019.100516
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页数：2
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