Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies.
- DOI
- 10.1016/j.kint.2017.10.016
- Published
- 2018 Apr
- Container
- Kidney international
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/j.kint.2017.10.016,
title = {Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies.},
author = {Ashton EJ and Legrand A and Benoit V and Roncelin I and Venisse A and Zennaro MC and Jeunemaitre X and Iancu D and Van't Hoff WG and Walsh SB and Godefroid N and Rotthier A and Del Favero J and Devuyst O and Schaefer F and Jenkins LA and Kleta R and Dahan K and Vargas-Poussou R and Bockenhauer D},
year = {2018},
journal = {Kidney international},
doi = {10.1016/j.kint.2017.10.016},
url = {https://doi.org/10.1016/j.kint.2017.10.016}
}RIS
TY - JOUR TI - Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies. AU - Ashton EJ AU - Legrand A AU - Benoit V AU - Roncelin I AU - Venisse A AU - Zennaro MC AU - Jeunemaitre X AU - Iancu D AU - Van't Hoff WG AU - Walsh SB AU - Godefroid N AU - Rotthier A AU - Del Favero J AU - Devuyst O AU - Schaefer F AU - Jenkins LA AU - Kleta R AU - Dahan K AU - Vargas-Poussou R AU - Bockenhauer D PY - 2018 JO - Kidney international DO - 10.1016/j.kint.2017.10.016 UR - https://doi.org/10.1016/j.kint.2017.10.016 ER -
APA
EJ, A., A, L., V, B., I, R., A, V., MC, Z., X, J., D, I., WG, V. H., SB, W., N, G., A, R., J, D. F., O, D., F, S., LA, J., R, K., K, D., R, V., & D, B. (2018). Simultaneous sequencing of 37 genes identified causative mutations in the majority of children with renal tubulopathies.. Kidney international. https://doi.org/10.1016/j.kint.2017.10.016
Source records
- pubmed · retrieved 2026-09-26T10:05:55.456Z