Left ventricular noncompaction

[1]. Aleksandra Nijak, et al. Left ventricular non-compaction with Ebstein anomaly attributed to a TPM1 mutation. Eur J Med Genet. 2018 Jan;61(1):8-10. [Content Brief]

[2]. Anne-Karin Arndt, et al. Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy. Am J Hum Genet. 2013 Jul 11;93(1):67-77. [Content Brief]

[3]. Erwin Oechslin, et al. Left ventricular non-compaction revisited: a distinct phenotype with genetic heterogeneity?. Eur Heart J. 2011 Jun;32(12):1446-56. [Content Brief]

[4]. Fukiko Ichida, et al. Left ventricular noncompaction. Circ J. 2009 Jan;73(1):19-26. [Content Brief]

[5]. Guillermo Luxán, et al. Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy. Nat Med. 2013 Feb;19(2):193-201. [Content Brief]

[6]. Lorenzo Monserrat, et al. Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects. Eur Heart J. 2007 Aug;28(16):1953-61. [Content Brief]

[7]. Mark Luedde, et al. Severe familial left ventricular non-compaction cardiomyopathy due to a novel troponin T (TNNT2) mutation. Cardiovasc Res. 2010 Jun 1;86(3):452-60. [Content Brief]

[8]. Matteo Vatta, et al. Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction. J Am Coll Cardiol. 2003 Dec 3;42(11):2014-27. [Content Brief]

[9]. Qing Cao, et al. Phenotype and Functional Analyses in a Transgenic Mouse Model of Left Ventricular Noncompaction Caused by a DTNA Mutation. Int Heart J. 2017 Dec 12;58(6):939-947. [Content Brief]

[10]. Sabine Klaassen, et al. Mutations in sarcomere protein genes in left ventricular noncompaction. Circulation. 2008 Jun 3;117(22):2893-901. [Content Brief]

[11]. Susanne Probst, et al. Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype. Circ Cardiovasc Genet. 2011 Aug 1;4(4):367-74. [Content Brief]