Nyegaard, M; Overgaard, MT; Søndergaard, MT; Vranas, M; Behr, ER; Hildebrandt, LL; Lund, J; Hedley, PL; Camm, AJ; Wettrell, G; et al. Nyegaard, M; Overgaard, MT; Søndergaard, MT; Vranas, M; Behr, ER; Hildebrandt, LL; Lund, J; Hedley, PL; Camm, AJ; Wettrell, G; Fosdal, I; Christiansen, M; Børglum, AD (2012) Mutations in Calmodulin Cause Ventricular Tachycardia and Sudden Cardiac Death. AMERICAN JOURNAL OF HUMAN GENETICS, 91 (4). 703 - 712 (10). ISSN 0002-9297 https://doi.org/10.1016/j.ajhg.2012.08.015
SGUL Authors: Behr, Elijah Raphael Camm, Alan John

Full text not available from this repository.

Item Type:	Article
Additional Information:	PubMed ID: 23040497
Keywords:	Adolescent, Adult, Amino Acid Sequence, Arrhythmias, Cardiac, Calcium Channels, Calmodulin, Child, Child, Preschool, Chromosomes, Human, Pair 14, Death, Sudden, Cardiac, Female, Genetic Predisposition to Disease, Heterozygote, Humans, Male, Molecular Sequence Data, Mutation, Missense, Ryanodine Receptor Calcium Release Channel, Syncope, Tachycardia, Ventricular, Young Adult, Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, RYANODINE RECEPTOR, CALCIUM-BINDING, CA2+ RELEASE, CHANNEL, COMPLEX, DIAGNOSIS, FAMILIES, CPVT, MAPS, TOOL
SGUL Research Institute / Research Centre:	Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) > Cardiac (INCCCA)
Journal or Publication Title:	AMERICAN JOURNAL OF HUMAN GENETICS
ISSN:	0002-9297
Dates:	Date Event 5 October 2012 Published
Web of Science ID:	WOS:000309568500012
	Download EPMC Full text (PDF)
	Download EPMC Full text (HTML)
URI:	https://openaccess.sgul.ac.uk/id/eprint/101655
Publisher's version:	https://doi.org/10.1016/j.ajhg.2012.08.015

Actions (login required)

Edit Item