A novel mutation in KVLQT1, L122P, found in a family with autosomal dominant long QT syndrome.

Krahn AD, Wang J, Spindler B, Skanes AC, Yee R, Klein GJ, Hegele RA.

DOI: 10.1067/mhj.2000.106599
Published: 2000-07-01
Container: Am Heart J
Publisher: Not recorded
Open access: no

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Cite this work

BibTeX

@article{allodium:10.1067/mhj.2000.106599,
  title = {A novel mutation in KVLQT1, L122P, found in a family with autosomal dominant long QT syndrome.},
  author = {Krahn AD and  Wang J and  Spindler B and  Skanes AC and  Yee R and  Klein GJ and  Hegele RA.},
  year = {2000},
  journal = {Am Heart J},
  doi = {10.1067/mhj.2000.106599},
  url = {https://doi.org/10.1067/mhj.2000.106599}
}

RIS

TY  - JOUR
TI  - A novel mutation in KVLQT1, L122P, found in a family with autosomal dominant long QT syndrome.
AU  - Krahn AD
AU  -  Wang J
AU  -  Spindler B
AU  -  Skanes AC
AU  -  Yee R
AU  -  Klein GJ
AU  -  Hegele RA.
PY  - 2000
JO  - Am Heart J
DO  - 10.1067/mhj.2000.106599
UR  - https://doi.org/10.1067/mhj.2000.106599
ER  -

APA

AD, K., J, W., B, S., AC, S., R, Y., GJ, K., & RA., H. (2000). A novel mutation in KVLQT1, L122P, found in a family with autosomal dominant long QT syndrome.. Am Heart J. https://doi.org/10.1067/mhj.2000.106599

Source records

europe-pmc · retrieved 2026-09-25T03:30:21.465Z