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Deficiency of mitochondrial ATP synthase of nuclear genetic origin

(2006) NEUROMUSCULAR DISORDERS. 16(12). p.821-829
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MLA
SPERL, W, P JESINA, J ZEMAN, et al. “Deficiency of Mitochondrial ATP Synthase of Nuclear Genetic Origin.” NEUROMUSCULAR DISORDERS 16.12 (2006): 821–829. Print.
APA
SPERL, W., JESINA, P., ZEMAN, J., MAYR, J., DEMEIRLEIR, L., Van Coster, R., PICKOVA, A., et al. (2006). Deficiency of mitochondrial ATP synthase of nuclear genetic origin. NEUROMUSCULAR DISORDERS, 16(12), 821–829.
Chicago author-date
SPERL, W, P JESINA, J ZEMAN, JA MAYR, L DEMEIRLEIR, Rudy Van Coster, A PICKOVA, et al. 2006. “Deficiency of Mitochondrial ATP Synthase of Nuclear Genetic Origin.” Neuromuscular Disorders 16 (12): 821–829.
Chicago author-date (all authors)
SPERL, W, P JESINA, J ZEMAN, JA MAYR, L DEMEIRLEIR, Rudy Van Coster, A PICKOVA, H HANSIKOVA, H HOUST’KOVA, Z KREJCIK, J KOCH, Joél Smet, W MUSS, E HOLME, and J HOUSTEK. 2006. “Deficiency of Mitochondrial ATP Synthase of Nuclear Genetic Origin.” Neuromuscular Disorders 16 (12): 821–829.
Vancouver
1.
SPERL W, JESINA P, ZEMAN J, MAYR J, DEMEIRLEIR L, Van Coster R, et al. Deficiency of mitochondrial ATP synthase of nuclear genetic origin. NEUROMUSCULAR DISORDERS. PERGAMON-ELSEVIER SCIENCE LTD; 2006;16(12):821–9.
IEEE
[1]
W. SPERL et al., “Deficiency of mitochondrial ATP synthase of nuclear genetic origin,” NEUROMUSCULAR DISORDERS, vol. 16, no. 12, pp. 821–829, 2006.
@article{369988,
  author       = {SPERL, W and JESINA, P and ZEMAN, J and MAYR, JA and DEMEIRLEIR, L and Van Coster, Rudy and PICKOVA, A and HANSIKOVA, H and HOUST'KOVA, H and KREJCIK, Z and KOCH, J and Smet, Joél and MUSS, W and HOLME, E and HOUSTEK, J},
  issn         = {0960-8966},
  journal      = {NEUROMUSCULAR DISORDERS},
  language     = {eng},
  number       = {12},
  pages        = {821--829},
  publisher    = {PERGAMON-ELSEVIER SCIENCE LTD},
  title        = {Deficiency of mitochondrial ATP synthase of nuclear genetic origin},
  volume       = {16},
  year         = {2006},
}

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