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Right ventricle late gadolinium enhancement in cardiac sarcoidosis: a case series

✍ Scribed by Carmen P Lydell; Iacopo Carbone; Naeem Merchant


Publisher
BioMed Central
Year
2011
Tongue
English
Weight
179 KB
Volume
13
Category
Article
ISSN
1097-6647

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## Abstract ## Background Miyoshi myopathy (MM) is an autosomal recessive distal myopathy characterized by early adult onset. Cardiomyopathy is a major clinical manifestation in other muscular dystrophies and an important prognostic factor. Although dysferlin is highly expressed in cardiac muscle,