Identification of partial SLC20A2 deletions in primary brain calcification using whole-exome sequencing.

David S, Ferreira J, Quenez O, Rovelet-Lecrux A, Richard AC, Vérin M, Jurici S, Le Ber I, Boland A, Deleuze JF, Frebourg T, Mendes de Oliveira JR, Hannequin D, Campion D, Nicolas G

Open source

DOI
10.1038/ejhg.2016.50
Published
2016 Nov
Container
European journal of human genetics : EJHG
Publisher
Not recorded
Open access
yes

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BibTeX

@article{allodium:10.1038/ejhg.2016.50,
  title = {Identification of partial SLC20A2 deletions in primary brain calcification using whole-exome sequencing.},
  author = {David S and Ferreira J and Quenez O and Rovelet-Lecrux A and Richard AC and Vérin M and Jurici S and Le Ber I and Boland A and Deleuze JF and Frebourg T and Mendes de Oliveira JR and Hannequin D and Campion D and Nicolas G},
  year = {2016},
  journal = {European journal of human genetics : EJHG},
  doi = {10.1038/ejhg.2016.50},
  url = {https://doi.org/10.1038/ejhg.2016.50}
}

RIS

TY  - JOUR
TI  - Identification of partial SLC20A2 deletions in primary brain calcification using whole-exome sequencing.
AU  - David S
AU  - Ferreira J
AU  - Quenez O
AU  - Rovelet-Lecrux A
AU  - Richard AC
AU  - Vérin M
AU  - Jurici S
AU  - Le Ber I
AU  - Boland A
AU  - Deleuze JF
AU  - Frebourg T
AU  - Mendes de Oliveira JR
AU  - Hannequin D
AU  - Campion D
AU  - Nicolas G
PY  - 2016
JO  - European journal of human genetics : EJHG
DO  - 10.1038/ejhg.2016.50
UR  - https://doi.org/10.1038/ejhg.2016.50
ER  - 

APA

S, D., J, F., O, Q., A, R., AC, R., M, V., S, J., I, L. B., A, B., JF, D., T, F., JR, M. D. O., D, H., D, C., & G, N. (2016). Identification of partial SLC20A2 deletions in primary brain calcification using whole-exome sequencing.. European journal of human genetics : EJHG. https://doi.org/10.1038/ejhg.2016.50

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