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Mitochondrial Short-Chain Enoyl-CoA Hydratase 1 Deficiency (ECHS1D)

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Genetic Syndromes

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Abstract

OMIM: 616277

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References

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Authors and Affiliations

  1. School of Life and Environmental Sciences, Faculty of Science, Engineering and Built Environment, Deakin University, Geelong, VIC, Australia

    Harrison J. Burgin & Matthew McKenzie

  2. Department of Metabolism, Chiba Children’s Hospital, Chiba, Japan

    Kei Murayama

  3. Department of Clinical Genomics & Pediatrics, Saitama Medical University, Saitama, Japan

    Akira Ohtake

Authors
  1. Harrison J. Burgin
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  2. Kei Murayama
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  3. Akira Ohtake
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  4. Matthew McKenzie
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Corresponding author

Correspondence to Matthew McKenzie .

Editor information

Editors and Affiliations

  1. Research Center for Immunodeficiencies, Children's Medical Center, Tehran University of Medical Sciences, Tehran, Iran

    Nima Rezaei

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Burgin, H.J., Murayama, K., Ohtake, A., McKenzie, M. (2022). Mitochondrial Short-Chain Enoyl-CoA Hydratase 1 Deficiency (ECHS1D). In: Rezaei, N. (eds) Genetic Syndromes. Springer, Cham. https://doi.org/10.1007/978-3-319-66816-1_1343-1

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  • DOI: https://doi.org/10.1007/978-3-319-66816-1_1343-1

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  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-319-66816-1

  • Online ISBN: 978-3-319-66816-1

  • eBook Packages: Springer Reference MedicineReference Module Medicine

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