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Gain-of-function mutations in TRPM4 cause autosomal dominant isolated cardiac conduction disease.

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Gain-of-function mutations in TRPM4 cause autosomal dominant isolated cardiac conduction disease. / Liu, Hui; Loubna, El Zein; Kruse, Martin; Guinamard, Romain; Beckmann, Alf; Bozio, André; Kurtbay, Güven; Mégarbané, André; Ohmert, Iris; Blaysat, Gérard; Villain, Elisabeth; Pongs, Olaf; Bouvagnet, Patrice.

in: CIRC-CARDIOVASC GENE, Jahrgang 3, Nr. 4, 4, 2010, S. 374-385.

Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung

Harvard

Liu, H, Loubna, EZ, Kruse, M, Guinamard, R, Beckmann, A, Bozio, A, Kurtbay, G, Mégarbané, A, Ohmert, I, Blaysat, G, Villain, E, Pongs, O & Bouvagnet, P 2010, 'Gain-of-function mutations in TRPM4 cause autosomal dominant isolated cardiac conduction disease.', CIRC-CARDIOVASC GENE, Jg. 3, Nr. 4, 4, S. 374-385. <http://www.ncbi.nlm.nih.gov/pubmed/20562447?dopt=Citation>

APA

Liu, H., Loubna, E. Z., Kruse, M., Guinamard, R., Beckmann, A., Bozio, A., Kurtbay, G., Mégarbané, A., Ohmert, I., Blaysat, G., Villain, E., Pongs, O., & Bouvagnet, P. (2010). Gain-of-function mutations in TRPM4 cause autosomal dominant isolated cardiac conduction disease. CIRC-CARDIOVASC GENE, 3(4), 374-385. [4]. http://www.ncbi.nlm.nih.gov/pubmed/20562447?dopt=Citation

Vancouver

Liu H, Loubna EZ, Kruse M, Guinamard R, Beckmann A, Bozio A et al. Gain-of-function mutations in TRPM4 cause autosomal dominant isolated cardiac conduction disease. CIRC-CARDIOVASC GENE. 2010;3(4):374-385. 4.

Bibtex

@article{33c7ae78a9154cec97d3b944e6b612da,
title = "Gain-of-function mutations in TRPM4 cause autosomal dominant isolated cardiac conduction disease.",
abstract = "Isolated cardiac conduction block is a relatively common condition in young and elderly populations. Genetic predisposing factors have long been suspected because of numerous familial case reports. Deciphering genetic predisposing factors of conduction blocks may give a hint at stratifying conduction block carriers in a more efficient way.",
author = "Hui Liu and Loubna, {El Zein} and Martin Kruse and Romain Guinamard and Alf Beckmann and Andr{\'e} Bozio and G{\"u}ven Kurtbay and Andr{\'e} M{\'e}garban{\'e} and Iris Ohmert and G{\'e}rard Blaysat and Elisabeth Villain and Olaf Pongs and Patrice Bouvagnet",
year = "2010",
language = "Deutsch",
volume = "3",
pages = "374--385",
journal = "CIRC-CARDIOVASC GENE",
issn = "1942-325X",
publisher = "Lippincott Williams and Wilkins",
number = "4",

}

RIS

TY - JOUR

T1 - Gain-of-function mutations in TRPM4 cause autosomal dominant isolated cardiac conduction disease.

AU - Liu, Hui

AU - Loubna, El Zein

AU - Kruse, Martin

AU - Guinamard, Romain

AU - Beckmann, Alf

AU - Bozio, André

AU - Kurtbay, Güven

AU - Mégarbané, André

AU - Ohmert, Iris

AU - Blaysat, Gérard

AU - Villain, Elisabeth

AU - Pongs, Olaf

AU - Bouvagnet, Patrice

PY - 2010

Y1 - 2010

N2 - Isolated cardiac conduction block is a relatively common condition in young and elderly populations. Genetic predisposing factors have long been suspected because of numerous familial case reports. Deciphering genetic predisposing factors of conduction blocks may give a hint at stratifying conduction block carriers in a more efficient way.

AB - Isolated cardiac conduction block is a relatively common condition in young and elderly populations. Genetic predisposing factors have long been suspected because of numerous familial case reports. Deciphering genetic predisposing factors of conduction blocks may give a hint at stratifying conduction block carriers in a more efficient way.

M3 - SCORING: Zeitschriftenaufsatz

VL - 3

SP - 374

EP - 385

JO - CIRC-CARDIOVASC GENE

JF - CIRC-CARDIOVASC GENE

SN - 1942-325X

IS - 4

M1 - 4

ER -