Diagnosis of riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency (MADD) by newborn screening: a feasibility study
碩士 === 國立臺灣大學 === 分子醫學研究所 === 102 === Background Glutaric acidemia type II (GA II), also known as multiple acyl-coenzyme A dehydrogenase de&;#64257;ciency (MADD), is an autosomal recessive disease caused by electron transfer flavoprotein (ETF) or electron transfer flavoprotein dehydrogenase (ETF...
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| Format: | Others |
| Language: | zh-TW |
| Published: |
2014
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| Online Access: | http://ndltd.ncl.edu.tw/handle/47038496439409571946 |