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Sudden death in a Korean infant with very long-chain acyl-CoA dehydrogenase deficiency

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Journal of Inherited Metabolic Disease

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REFERENCES

  • Hahn SH, Lee EH, Jung JW, et al (1999) Very long chain acyl coenzyme A dehydrogenase deficiency in a 5-month-old Korean boy: identification of a novel mutation. J Pediatr 135: 250-253.

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  • Mathur A, Sills HP, Gopalalkrishnan D, et al (1999) Molecular heterogeneity in very-long chain acyl-CoA dehydrogenase deficiency causing pediatric cardiomyopathy and sudden death. Circulation 99: 1337-1343.

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  • Strauss AW, Powell CK, Hale DR, et al (1995) Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood. Proc Natl Acad Sci USA 92: 10496-10500.

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Authors and Affiliations

  1. Metabolic Disease Detection Laboratory, Seoul Medical Science Institute, Korea

    H.-R. Yoon

  2. Department of Pediatrics, Medical Center North Nashville, Vanderbilt University, Tennessee, USA

    A. W. Strauss

  3. Department of Pediatrics, Asan Medical Center, Ulsan University College of Medicine, 388-1 Pungnap-Dong, Songpa-Gu, Seoul, 138-736, Korea

    H.-W. Yoo

Authors
  1. H.-R. Yoon
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  2. A. W. Strauss
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  3. H.-W. Yoo
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Yoon, HR., Strauss, A.W. & Yoo, HW. Sudden death in a Korean infant with very long-chain acyl-CoA dehydrogenase deficiency. J Inherit Metab Dis 24, 407–408 (2001). https://doi.org/10.1023/A:1010521105909

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  • DOI: https://doi.org/10.1023/A:1010521105909

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