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KMID : 0918520020020010012
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Journal of the Korean Society of Inherited Metabolic Disease
2002 Volume.2 No. 1 p.12 ~ p.14
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The First Case of Korean Boy with Mitochondrial Trifunctional Protein Deficiency Diagnosed by Acylcarnitine profiles and DNA analysis : A Novel Mutation in the α-subunit of the Mitochondrial Trifunctional Protein and a Unusual Intergenic Sequence with Tw
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이지은
윤혜란/백경훈/황종희/황수정/심재원/장윤실/박원순/Strauss AW/진동규/Lee JE/Yoon HR/Paik KH/Hwang JH/Hwang SJ/Shim JW/Chang YS/Park WS/Jin DK
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Abstract
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KEYWORD
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