A rare case of familial restrictive cardiomyopathy, with mutations in MYH7 and ABCC9 genes. [electronic resource]

By: Contributor(s): Publication details: Discoveries (Craiova, Romania) Sep 2019Description: e99 p. digitalISSN:
  • 2359-7232
Online resources: In: Discoveries (Craiova, Romania) vol. 7
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Publication Type: Journal Article

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