Clinical and molecular genetic risk determinants in adult long QT syndrome type 1 and 2 patients : Koponen et al. Follow-up of adult LQTS patients.

Koponen M, Havulinna AS, Marjamaa A, Tuiskula AM, Salomaa V, Laitinen-Forsblom PJ, Piippo K, Toivonen L, Kontula K, Viitasalo M, Swan H

Open source

DOI: 10.1186/s12881-018-0574-0
Published: 2018 Apr 5
Container: BMC medical genetics
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1186/s12881-018-0574-0,
  title = {Clinical and molecular genetic risk determinants in adult long QT syndrome type 1 and 2 patients : Koponen et al. Follow-up of adult LQTS patients.},
  author = {Koponen M and Havulinna AS and Marjamaa A and Tuiskula AM and Salomaa V and Laitinen-Forsblom PJ and Piippo K and Toivonen L and Kontula K and Viitasalo M and Swan H},
  year = {2018},
  journal = {BMC medical genetics},
  doi = {10.1186/s12881-018-0574-0},
  url = {https://doi.org/10.1186/s12881-018-0574-0}
}

RIS

TY  - JOUR
TI  - Clinical and molecular genetic risk determinants in adult long QT syndrome type 1 and 2 patients : Koponen et al. Follow-up of adult LQTS patients.
AU  - Koponen M
AU  - Havulinna AS
AU  - Marjamaa A
AU  - Tuiskula AM
AU  - Salomaa V
AU  - Laitinen-Forsblom PJ
AU  - Piippo K
AU  - Toivonen L
AU  - Kontula K
AU  - Viitasalo M
AU  - Swan H
PY  - 2018
JO  - BMC medical genetics
DO  - 10.1186/s12881-018-0574-0
UR  - https://doi.org/10.1186/s12881-018-0574-0
ER  -

APA

M, K., AS, H., A, M., AM, T., V, S., PJ, L., K, P., L, T., K, K., M, V., & H, S. (2018). Clinical and molecular genetic risk determinants in adult long QT syndrome type 1 and 2 patients : Koponen et al. Follow-up of adult LQTS patients.. BMC medical genetics. https://doi.org/10.1186/s12881-018-0574-0

Source records

pubmed · retrieved 2026-09-26T18:06:03.678Z