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Complex III deficiency due to a homozygous mutation in the nuclear encoded subunit UQCRQ

Rudy Van Coster (UGent) , Joél Smet (UGent) , Boel De Paepe (UGent) , Elise Vantroys (UGent) , Femke Nachtergaele (UGent) , Sarah Vergult (UGent) , Björn Menten (UGent) , Arnaud Vanlander (UGent) and François-Guillaume Debray
(2018) In JOURNAL OF INHERITED METABOLIC DISEASE 41(suppl. 1). p.S153-S153
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MLA
Van Coster, Rudy, Joél Smet, Boel De Paepe, et al. “Complex III Deficiency Due to a Homozygous Mutation in the Nuclear Encoded Subunit UQCRQ.” Vol. 41. 2018. S153–S153. Print.
APA
Van Coster, R., Smet, J., De Paepe, B., Vantroys, E., Nachtergaele, F., Vergult, S., Menten, B., et al. (2018). Complex III deficiency due to a homozygous mutation in the nuclear encoded subunit UQCRQ (Vol. 41, pp. S153–S153). Presented at the 2018 Annual symposium of the Society for the Study of Inborn Errors of Metabolism (SSIEM).
Chicago author-date
Van Coster, Rudy, Joél Smet, Boel De Paepe, Elise Vantroys, Femke Nachtergaele, Sarah Vergult, Björn Menten, Arnaud Vanlander, and François-Guillaume Debray. 2018. “Complex III Deficiency Due to a Homozygous Mutation in the Nuclear Encoded Subunit UQCRQ.” In , 41:S153–S153.
Chicago author-date (all authors)
Van Coster, Rudy, Joél Smet, Boel De Paepe, Elise Vantroys, Femke Nachtergaele, Sarah Vergult, Björn Menten, Arnaud Vanlander, and François-Guillaume Debray. 2018. “Complex III Deficiency Due to a Homozygous Mutation in the Nuclear Encoded Subunit UQCRQ.” In , 41:S153–S153.
Vancouver
1.
Van Coster R, Smet J, De Paepe B, Vantroys E, Nachtergaele F, Vergult S, et al. Complex III deficiency due to a homozygous mutation in the nuclear encoded subunit UQCRQ. 2018. p. S153–S153.
IEEE
[1]
R. Van Coster et al., “Complex III deficiency due to a homozygous mutation in the nuclear encoded subunit UQCRQ,” presented at the 2018 Annual symposium of the Society for the Study of Inborn Errors of Metabolism (SSIEM), Athene, Greece, 2018, vol. 41, no. suppl. 1, pp. S153–S153.
@inproceedings{8573432,
  author       = {Van Coster, Rudy and Smet, Joél and De Paepe, Boel and Vantroys, Elise and Nachtergaele, Femke and Vergult, Sarah and Menten, Björn and Vanlander, Arnaud and Debray, François-Guillaume},
  issn         = {0141-8955},
  language     = {eng},
  location     = {Athene, Greece},
  number       = {suppl. 1},
  pages        = {S153--S153},
  title        = {Complex III deficiency due to a homozygous mutation in the nuclear encoded subunit UQCRQ},
  volume       = {41},
  year         = {2018},
}