Fig. 2From: A case report of recessive restrictive cardiomyopathy caused by a novel mutation in cardiac troponin I (TNNI3)The histology of the affected myocardium revealed multiple foci of intestitial and pericellurar fibrosis with features of non-specific myocytic hypertrophy. There was no evidence of inflammation or deposition of amyloid. (trichrome stain Χ100)Back to article page