Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: Implications for acquired and congenital long QT syndrome

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Standard

Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: Implications for acquired and congenital long QT syndrome. / Larsen, Lars Allan; Andersen, Paal Skytt; Kanters, Jørgen K.; Svendsen, Ida Hastrup; Jacobsen, J.R.; Vuust, J.; Wetrell, G.; Tranebjærg, Lisbeth; Christiansen, M.

In: Clinical Chemistry, Vol. 47, No. 8, 2001, p. 1390-1395.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Larsen, LA, Andersen, PS, Kanters, JK, Svendsen, IH, Jacobsen, JR, Vuust, J, Wetrell, G, Tranebjærg, L & Christiansen, M 2001, 'Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: Implications for acquired and congenital long QT syndrome', Clinical Chemistry, vol. 47, no. 8, pp. 1390-1395.

APA

Larsen, L. A., Andersen, P. S., Kanters, J. K., Svendsen, I. H., Jacobsen, J. R., Vuust, J., Wetrell, G., Tranebjærg, L., & Christiansen, M. (2001). Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: Implications for acquired and congenital long QT syndrome. Clinical Chemistry, 47(8), 1390-1395.

Vancouver

Larsen LA, Andersen PS, Kanters JK, Svendsen IH, Jacobsen JR, Vuust J et al. Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: Implications for acquired and congenital long QT syndrome. Clinical Chemistry. 2001;47(8):1390-1395.

Author

Larsen, Lars Allan ; Andersen, Paal Skytt ; Kanters, Jørgen K. ; Svendsen, Ida Hastrup ; Jacobsen, J.R. ; Vuust, J. ; Wetrell, G. ; Tranebjærg, Lisbeth ; Christiansen, M. / Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: Implications for acquired and congenital long QT syndrome. In: Clinical Chemistry. 2001 ; Vol. 47, No. 8. pp. 1390-1395.

Bibtex

@article{fc00e25074c411dbbee902004c4f4f50,
title = "Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: Implications for acquired and congenital long QT syndrome",
author = "Larsen, {Lars Allan} and Andersen, {Paal Skytt} and Kanters, {J{\o}rgen K.} and Svendsen, {Ida Hastrup} and J.R. Jacobsen and J. Vuust and G. Wetrell and Lisbeth Tranebj{\ae}rg and M. Christiansen",
year = "2001",
language = "English",
volume = "47",
pages = "1390--1395",
journal = "Clinical Chemistry",
issn = "0009-9147",
publisher = "American Association for Clinical Chemistry, Inc.",
number = "8",

}

RIS

TY - JOUR

T1 - Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: Implications for acquired and congenital long QT syndrome

AU - Larsen, Lars Allan

AU - Andersen, Paal Skytt

AU - Kanters, Jørgen K.

AU - Svendsen, Ida Hastrup

AU - Jacobsen, J.R.

AU - Vuust, J.

AU - Wetrell, G.

AU - Tranebjærg, Lisbeth

AU - Christiansen, M.

PY - 2001

Y1 - 2001

M3 - Journal article

VL - 47

SP - 1390

EP - 1395

JO - Clinical Chemistry

JF - Clinical Chemistry

SN - 0009-9147

IS - 8

ER -

ID: 122675