Journal of The Korean Society of Inherited Metabolic disease (대한유전성대사질환학회지)
- Volume 1 Issue 1
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- Pages.28-29
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- 2001
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- 2287-4712(pISSN)
Sudden Infant Death in the Second Case of Korean Girl with Very Long Chain Acyl CoA Dehydrogenase (VLCAD) Deficiency
- Yoon, Hye-Ran (Metabolic Disease Detection Laboratory, Seoul Medical Science Institute) ;
- Strauss, Arnold W (St.Louis Children's Hospital, One Children's place) ;
- Yoo, Han-Wook (Department of Pediatrics, Asan Medical Center, Ulsan University College of Medicine)
- Published : 2001.05.01
Abstract
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