Development of Molecular Techniques for Identification of β-Thalassemia Mutations
博士 === 國立中興大學 === 獸醫學系暨研究所 === 97 === Thalassemia is clinically heterogeneous because various genetic lesions variably impair globin-chain synthesis. β-thalassemia is one of the most common genetic diseases in the world. It is an autosomal recessive inherited disease resulting from point mutations,...
| Main Authors: | , |
|---|---|
| Other Authors: | |
| Format: | Others |
| Language: | zh-TW |
| Published: |
2009
|
| Online Access: | http://ndltd.ncl.edu.tw/handle/82159874511741557697 |