Therapeutic Potential of αS Evolvability for Neuropathic Gaucher Disease
Gaucher disease (GD), the most common lysosomal storage disorder (LSD), is caused by autosomal recessive mutations of the glucocerebrosidase gene, <i>GBA1</i>. In the majority of cases, GD has a non-neuropathic chronic form with adult onset (GD1), while other cases are more acute and sev...
| Main Authors: | , , , , , , |
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| 格式: | 文件 |
| 语言: | English |
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MDPI AG
2021-02-01
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| 丛编: | Biomolecules |
| 主题: | |
| 在线阅读: | https://www.mdpi.com/2218-273X/11/2/289 |