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pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov

Case Report: Restrictive cardiomyopathy due to a rare mutation in troponin I gene (TNNI3) in a patient

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1. ClingenBaseline 02 Nov 2026
  
  in Baseline Annotations
  
  Case Report: Restrictive cardiomyopathy due to a rare mutation in troponin I gene (TNNI3) in a patient
  
  Gene:TNNI3 PMID:39635265 HGNC ID:11947 inferred_gene_hgnc:11947 inferred_gene_source:HGNC_body Cardiomyopathy Annotation
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Tags

PMID:39635265

inferred_gene_source:HGNC_body

inferred_gene_hgnc:11947

Cardiomyopathy Annotation

HGNC ID:11947

Gene:TNNI3

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ClingenBaseline

URL

pmc.ncbi.nlm.nih.gov/articles/PMC11614833/