Lack of evidence for a causal role of CALR3 in monogenic cardiomyopathy-Reference-Cited by-同舟云学术

Lack of evidence for a causal role of CALR3 in monogenic cardiomyopathy

Published:2018-07-09 Issue:11 Volume:26 Page:1603-1610
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Verhagen Judith M. A.^ORCID,Veldman Job H.,van der Zwaag Paul A.,von der Thüsen Jan H.,Brosens Erwin^ORCID,Christiaans Imke,Dooijes Dennis,Helderman-van den Enden Apollonia T. J. M.,Lekanne Deprez Ronald H.,Michels Michelle,van Mil Anneke M.^ORCID,Oldenburg Rogier A.,van der Smagt Jasper J.,van den Wijngaard Arthur,Wessels Marja W.,Hofstra Robert M. W.,van Slegtenhorst Marjon A.,Jongbloed Jan D. H.,van de Laar Ingrid M. B. H.

Funder

Hartstichting (Dutch Heart Foundation)

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/s41431-018-0208-1.pdf

Reference27 articles.

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2. Chiu C, Tebo M, Ingles J, et al. Genetic screening of calcium regulation genes in familial hypertrophic cardiomyopathy. J Mol Cell Cardiol. 2007;43:337–43.

3. Nomura R, Orii M, Senda T. Calreticulin-2 is localized in the lumen of the endoplasmic reticulum but is not a Ca2+-binding protein. Histochem Cell Biol. 2011;135:531–8.