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Fig. 2 | BMC Medical Genetics

Fig. 2

From: Establishing disease causality for a novel gene variant in familial dilated cardiomyopathy using a functional in-vitro assay of regulated thin filaments and human cardiac myosin

Fig. 2

Transthoracic echocardiographic 4 chamber views (a, b) and m-mode at the level of the mitral valve (c, d) of the II-2 unaffected sibling (a, c) and the II-3 proband (b, d). A severely dilated left ventricle with poor systolic function is noted in the proband, while the unaffected sibling has normal cavity size and normal systolic function

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