Muggenthaler, M; Petropoulou, E; Omer, S; Simpson, MA; Sahak, H; Rice, A; Raju, H; Conti, FJ; Bridges, LR; Anderson, LJ; et al. Muggenthaler, M; Petropoulou, E; Omer, S; Simpson, MA; Sahak, H; Rice, A; Raju, H; Conti, FJ; Bridges, LR; Anderson, LJ; Sharma, S; Behr, ER; Jamshidi, Y (2016) Whole exome sequence analysis reveals a homozygous mutation in PNPLA2 as the cause of severe dilated cardiomyopathy secondary to neutral lipid storage disease. International Journal of Cardiology, 210. pp. 41-44. https://doi.org/10.1016/j.ijcard.2016.02.082
SGUL Authors: Behr, Elijah Raphael Jamshidi, Yalda Raju, Hariharan Sharma, Sanjay

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Item Type:	Article
Additional Information:	© 2016 Elsevier Ireland Ltd. All rights reserved.
Keywords:	ATGL, Cardiomyopathy, Exome, Muscle, NLSD-M, PNPLA2, Cardiovascular System & Hematology, 1102 Cardiovascular Medicine And Haematology
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) Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) > Cell Sciences (INCCCS)
Journal or Publication Title:	International Journal of Cardiology
Language:	ENG
Dates:	Date Event 13 February 2016 Published
Publisher License:	Creative Commons: Attribution-Noncommercial-No Derivative Works 4.0
Projects:	Project ID Funder Funder ID UNSPECIFIED St. George's, University of London http://dx.doi.org/10.13039/501100004337 UNSPECIFIED National Institute for Health Research http://dx.doi.org/10.13039/501100000272
PubMed ID:	26922712
	Go to PubMed abstract
URI:	https://openaccess.sgul.ac.uk/id/eprint/107736
Publisher's version:	https://doi.org/10.1016/j.ijcard.2016.02.082

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