Molecular Cloning and Functional Study of Acid Alpha-Glucosidase L291P Mutation in Pompe Disease
碩士 === 慈濟大學 === 分子生物暨人類遺傳學系碩士班 === 101 === Pompe disease (also known as glycogen storage disease type II; GSD-II) is a rare autosomal recessive disease which had an incidence of approximately 1 in 40,000 according statistics reported in Pompe Disease Newborn Screening Program by National Taiwan Uni...
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| Format: | Others |
| Language: | zh-TW |
| Published: |
2013
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| Online Access: | http://ndltd.ncl.edu.tw/handle/13321723644625134226 |