History of glycogen storage disease type Ⅱ
Glycogen storage disease type Ⅱ (GSD Ⅱ), which is also called Pompe disease, is an autosomal recessive hereditary metabolic disease resulting from mutations of acid α-glucosidase (GAA). GSD Ⅱ is characterized by involvements of skeletal muscle and cardiac muscle. It has been 85 years since the disco...
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| Huvudupphov: | , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Utgiven: |
Tianjin Huanhu Hospital
2018-08-01
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| Serie: | Chinese Journal of Contemporary Neurology and Neurosurgery |
| Ämnen: | |
| Länkar: | http://www.cjcnn.org/index.php/cjcnn/article/view/1818 |
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