Molecular genetic study of Pompe disease in Chinese patients in Taiwan
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference26 articles.
1. 1995. Glycogen storage disease. In: editors. The metabolic and molecular basis of inherited disease. New York: McGraw-Hill. p 935-965.
2. Identification of a point mutation in the human lysosomal α-glucosidase gene causing infantile glycogenosis type II
3. Human lysosomal alpha-glucosidase. Characterization of the catalytic site
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