Restrictive cardiomyopathy
Definition:
References:
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[1]. Aldrin V Gomes, et al. Molecular and cellular aspects of troponin cardiomyopathies. Ann N Y Acad Sci. 2004 May;1015:214-24. [Content Brief]
[2]. Andreas Brodehl, et al. Mutations in FLNC are Associated with Familial Restrictive Cardiomyopathy. Hum Mutat. 2016 Mar;37(3):269-79. [Content Brief]
[3]. Enkhsaikhan Purevjav, et al. Molecular basis for clinical heterogeneity in inherited cardiomyopathies due to myopalladin mutations. Hum Mol Genet. 2012 May 1;21(9):2039-53. [Content Brief]
[4]. J P Kaski, et al. Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes. Heart. 2008 Nov;94(11):1478-84. [Content Brief]
[5]. Jacoba J Louw, et al. Compound heterozygous loss-of-function mutations in KIF20A are associated with a novel lethal congenital cardiomyopathy in two siblings. PLoS Genet. 2018 Jan 22;14(1):e1007138. [Content Brief]
[6]. Michelle S Parvatiyar, et al. Cardiac troponin mutations and restrictive cardiomyopathy. J Biomed Biotechnol. 2010;2010:350706. [Content Brief]
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