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New mitochondrial diagnostic testing in fibroblasts, a minimally invasive tissue, identifies sensitive functional testing methods for complex I deficient primary mitochondrial disorders

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MLA
Knight, Kaz, Marisa W Friederich, Rudy Van Coster, et al. “New Mitochondrial Diagnostic Testing in Fibroblasts, a Minimally Invasive Tissue, Identifies Sensitive Functional Testing Methods for Complex I Deficient Primary Mitochondrial Disorders.” Molecular Genetics and Metabolism. Vol. 123. 2018. 202–202. Print.
APA
Knight, K., Friederich, M. W., Van Coster, R., Smet, J., Vantroys, E., Hirano, M., Goldstein, A., et al. (2018). New mitochondrial diagnostic testing in fibroblasts, a minimally invasive tissue, identifies sensitive functional testing methods for complex I deficient primary mitochondrial disorders. MOLECULAR GENETICS AND METABOLISM (Vol. 123, pp. 202–202). Presented at the 40th Annual meeting of the Society for Inherited Metabolic Disorders (SIMD).
Chicago author-date
Knight, Kaz, Marisa W Friederich, Rudy Van Coster, Joél Smet, Elise Vantroys, Michio Hirano, Amy Goldstein, and Johan LK Van Hove. 2018. “New Mitochondrial Diagnostic Testing in Fibroblasts, a Minimally Invasive Tissue, Identifies Sensitive Functional Testing Methods for Complex I Deficient Primary Mitochondrial Disorders.” In Molecular Genetics and Metabolism, 123:202–202.
Chicago author-date (all authors)
Knight, Kaz, Marisa W Friederich, Rudy Van Coster, Joél Smet, Elise Vantroys, Michio Hirano, Amy Goldstein, and Johan LK Van Hove. 2018. “New Mitochondrial Diagnostic Testing in Fibroblasts, a Minimally Invasive Tissue, Identifies Sensitive Functional Testing Methods for Complex I Deficient Primary Mitochondrial Disorders.” In Molecular Genetics and Metabolism, 123:202–202.
Vancouver
1.
Knight K, Friederich MW, Van Coster R, Smet J, Vantroys E, Hirano M, et al. New mitochondrial diagnostic testing in fibroblasts, a minimally invasive tissue, identifies sensitive functional testing methods for complex I deficient primary mitochondrial disorders. MOLECULAR GENETICS AND METABOLISM. 2018. p. 202–202.
IEEE
[1]
K. Knight et al., “New mitochondrial diagnostic testing in fibroblasts, a minimally invasive tissue, identifies sensitive functional testing methods for complex I deficient primary mitochondrial disorders,” in MOLECULAR GENETICS AND METABOLISM, San Diego, CA, USA, 2018, vol. 123, no. 3, pp. 202–202.
@inproceedings{8573430,
  author       = {Knight, Kaz and Friederich, Marisa W and Van Coster, Rudy and Smet, Joél and Vantroys, Elise and Hirano, Michio and Goldstein, Amy and Van Hove, Johan LK},
  booktitle    = {MOLECULAR GENETICS AND METABOLISM},
  issn         = {1096-7192},
  language     = {eng},
  location     = {San Diego, CA, USA},
  number       = {3},
  pages        = {202--202},
  title        = {New mitochondrial diagnostic testing in fibroblasts, a minimally invasive tissue, identifies sensitive functional testing methods for complex I deficient primary mitochondrial disorders},
  url          = {http://dx.doi.org/10.1016/j.ymgme.2017.12.430},
  volume       = {123},
  year         = {2018},
}

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