Global characterization of copy number variants in epilepsy patients from whole genome sequencing.

Monlong J, Girard SL, Meloche C, Cadieux-Dion M, Andrade DM, Lafreniere RG, Gravel M, Spiegelman D, Dionne-Laporte A, Boelman C, Hamdan FF, Michaud JL, Rouleau G, Minassian BA, Bourque G, Cossette P

Open source

DOI: 10.1371/journal.pgen.1007285
Published: 2018 Apr
Container: PLoS genetics
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1371/journal.pgen.1007285,
  title = {Global characterization of copy number variants in epilepsy patients from whole genome sequencing.},
  author = {Monlong J and Girard SL and Meloche C and Cadieux-Dion M and Andrade DM and Lafreniere RG and Gravel M and Spiegelman D and Dionne-Laporte A and Boelman C and Hamdan FF and Michaud JL and Rouleau G and Minassian BA and Bourque G and Cossette P},
  year = {2018},
  journal = {PLoS genetics},
  doi = {10.1371/journal.pgen.1007285},
  url = {https://doi.org/10.1371/journal.pgen.1007285}
}

RIS

TY  - JOUR
TI  - Global characterization of copy number variants in epilepsy patients from whole genome sequencing.
AU  - Monlong J
AU  - Girard SL
AU  - Meloche C
AU  - Cadieux-Dion M
AU  - Andrade DM
AU  - Lafreniere RG
AU  - Gravel M
AU  - Spiegelman D
AU  - Dionne-Laporte A
AU  - Boelman C
AU  - Hamdan FF
AU  - Michaud JL
AU  - Rouleau G
AU  - Minassian BA
AU  - Bourque G
AU  - Cossette P
PY  - 2018
JO  - PLoS genetics
DO  - 10.1371/journal.pgen.1007285
UR  - https://doi.org/10.1371/journal.pgen.1007285
ER  -

APA

J, M., SL, G., C, M., M, C., DM, A., RG, L., M, G., D, S., A, D., C, B., FF, H., JL, M., G, R., BA, M., G, B., & P, C. (2018). Global characterization of copy number variants in epilepsy patients from whole genome sequencing.. PLoS genetics. https://doi.org/10.1371/journal.pgen.1007285

Source records

pubmed · retrieved 2026-11-10T07:47:29.095Z