Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patients.
- DOI
- 10.1080/07853890600756065
- Published
- 2006
- Container
- Annals of medicine
- Publisher
- Not recorded
- Open access
- no
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Cite this work
BibTeX
@article{allodium:10.1080/07853890600756065,
title = {Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patients.},
author = {Fodstad H and Bendahhou S and Rougier JS and Laitinen-Forsblom PJ and Barhanin J and Abriel H and Schild L and Kontula K and Swan H},
year = {2006},
journal = {Annals of medicine},
doi = {10.1080/07853890600756065},
url = {https://doi.org/10.1080/07853890600756065}
}RIS
TY - JOUR TI - Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patients. AU - Fodstad H AU - Bendahhou S AU - Rougier JS AU - Laitinen-Forsblom PJ AU - Barhanin J AU - Abriel H AU - Schild L AU - Kontula K AU - Swan H PY - 2006 JO - Annals of medicine DO - 10.1080/07853890600756065 UR - https://doi.org/10.1080/07853890600756065 ER -
APA
H, F., S, B., JS, R., PJ, L., J, B., H, A., L, S., K, K., & H, S. (2006). Molecular characterization of two founder mutations causing long QT syndrome and identification of compound heterozygous patients.. Annals of medicine. https://doi.org/10.1080/07853890600756065
Source records
- pubmed · retrieved 2026-09-26T04:15:33.057Z
- europe-pmc · retrieved 2026-09-26T04:15:33.060Z
- hal · retrieved 2026-09-26T04:15:33.107Z