Case Report: Mutation in TNNI3(c. 544G>A): a novel likely pathogenic mechanism of neonatal dilated cardiomyopathy
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pubmed.ncbi.nlm.nih.gov pubmed.ncbi.nlm.nih.gov
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pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov
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Case Report: Restrictive cardiomyopathy due to a rare mutation in troponin I gene (TNNI3) in a patient
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