Human Genetic Diseases:Part I: Molecular and genetic studies of the IDS gene associated with mucopolysaccharidosis type II. Part II: Characterization of LDL Receptor Gene Mutations in Familial Hypercholesterolemia.
博士 === 國立臺灣師範大學 === 生物學系 === 93 === Part I: Molecular and genetic studies of the IDS gene associated with mucopolysaccharidosis type II Abstract Hunter syndrome (mucopolysaccharidosis type II) is an X-linked recessive lysosomal storage disease caused by a defect of the iduronate-2-sulfatase (IDS)...
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| Format: | Others |
| Language: | zh-TW |
| Online Access: | http://ndltd.ncl.edu.tw/handle/ytsaqg |