## Communicated by Elizabeth Neufeld Patients with glycogen storage disease type II (GSDII, Pompe disease) suffer from progressive muscle weakness due to acid a-glucosidase deficiency. The disease is inherited as an autosomal recessive trait with a spectrum of clinical phenotypes. We have investiga
β¦ LIBER β¦
Genotype-Phenotype Correlation in Two Frequent Mutations and Mutation Update in Type III Glycogen Storage Disease
β Scribed by Wen-Ling Shaiu; Priya S. Kishnani; Jianjun Shen; Hui-Ming Liu; Yuan-Tsong Chen
- Book ID
- 115639635
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 117 KB
- Volume
- 69
- Category
- Article
- ISSN
- 1096-7192
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