The clinical heterogeneity of the NARS2 c.822G>C mutation clearly illustrated in two siblings : epilepsy and myopathy
- Author
- Arnaud Vanlander (UGent) , Helene Verhelst (UGent) , Elise Vantroys (UGent) , Joél Smet (UGent) , Boel De Paepe (UGent) , Sarah Vergult (UGent) , Björn Menten (UGent) and Rudy Van Coster (UGent)
- Organization
Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-8573438
- MLA
- Vanlander, Arnaud, HELENE VERHELST, Elise Vantroys, et al. “The Clinical Heterogeneity of the NARS2 c.822G>C Mutation Clearly Illustrated in Two Siblings : Epilepsy and Myopathy.” Vol. 41. 2018. S156–S156. Print.
- APA
- Vanlander, Arnaud, VERHELST, H., Vantroys, E., Smet, J., De Paepe, B., Vergult, S., Menten, B., et al. (2018). The clinical heterogeneity of the NARS2 c.822G>C mutation clearly illustrated in two siblings : epilepsy and myopathy (Vol. 41, pp. S156–S156). Presented at the 2018 Annual symposium of the Society for the Study of Inborn Errors of Metabolism (SSIEM).
- Chicago author-date
- Vanlander, Arnaud, HELENE VERHELST, Elise Vantroys, Joél Smet, Boel De Paepe, Sarah Vergult, Björn Menten, and Rudy Van Coster. 2018. “The Clinical Heterogeneity of the NARS2 c.822G>C Mutation Clearly Illustrated in Two Siblings : Epilepsy and Myopathy.” In , 41:S156–S156.
- Chicago author-date (all authors)
- Vanlander, Arnaud, HELENE VERHELST, Elise Vantroys, Joél Smet, Boel De Paepe, Sarah Vergult, Björn Menten, and Rudy Van Coster. 2018. “The Clinical Heterogeneity of the NARS2 c.822G>C Mutation Clearly Illustrated in Two Siblings : Epilepsy and Myopathy.” In , 41:S156–S156.
- Vancouver
- 1.Vanlander A, VERHELST H, Vantroys E, Smet J, De Paepe B, Vergult S, et al. The clinical heterogeneity of the NARS2 c.822G>C mutation clearly illustrated in two siblings : epilepsy and myopathy. 2018. p. S156–S156.
- IEEE
- [1]A. Vanlander et al., “The clinical heterogeneity of the NARS2 c.822G>C mutation clearly illustrated in two siblings : epilepsy and myopathy,” presented at the 2018 Annual symposium of the Society for the Study of Inborn Errors of Metabolism (SSIEM), Athens, Greece, 2018, vol. 41, no. suppl. 1, pp. S156–S156.
@inproceedings{8573438,
author = {Vanlander, Arnaud and Verhelst, Helene and Vantroys, Elise and Smet, Joél and De Paepe, Boel and Vergult, Sarah and Menten, Björn and Van Coster, Rudy},
issn = {0141-8955},
language = {eng},
location = {Athens, Greece},
number = {suppl. 1},
pages = {S156--S156},
title = {The clinical heterogeneity of the NARS2 c.822G>C mutation clearly illustrated in two siblings : epilepsy and myopathy},
volume = {41},
year = {2018},
}