Newborn Screening Case Study of CBS Gene Defect-Case Based on Household Registration in Taitung
碩士 === 臺灣大學 === 分子醫學研究所 === 98 === Background: A mutation of the CBS gene associated with classical homocystinuria been discovered in Taiwan. The high incidence of the gene however, is inconsistent with results of neonatal screening, indicating that the sensitivity of the current protocol (methionin...
| Main Authors: | , |
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| Other Authors: | |
| Format: | Others |
| Language: | zh-TW |
| Published: |
2010
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| Online Access: | http://ndltd.ncl.edu.tw/handle/34060816272724463703 |