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UnknownCompound Heterozygous FKTN Variants in a Patient with Dilated Cardiomyopathy Led to an Aberrant α-Dystroglycan Pattern.
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S-EPMC9223741 | biostudies-literature
UnknownHemi- and Homozygous Loss-of-Function Mutations in DSG2 (Desmoglein-2) Cause Recessive Arrhythmogenic Cardiomyopathy with an Early Onset.
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S-EPMC8038858 | biostudies-literature
UnknownPathogenic Variants in Cardiomyopathy Disorder Genes Underlie Pediatric Myocarditis-Further Impact of Heterozygous Immune Disorder Gene Variants?
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S-EPMC9321514 | biostudies-literature
UnknownCase Report: Early Transplant Rejection of a Methanol-Intoxicated Donor Heart in a Young Female Patient. A Diagnostic Approach With CMR, Cardiac Biopsy, and Genetic Risk Assessment.
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S-EPMC7938323 | biostudies-literature
UnknownBlood taken immediately after fatal resuscitation attempts yields higher quality DNA for genetic studies as compared to autopsy samples.
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S-EPMC10421769 | biostudies-literature
UnknownMolecular autopsy and family screening in a young case of sudden cardiac death reveals an unusually severe case of FHL1 related hypertrophic cardiomyopathy.
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S-EPMC6687666 | biostudies-literature
UnknownDe Novo Missense Mutations in TNNC1 and TNNI3 Causing Severe Infantile Cardiomyopathy Affect Myofilament Structure and Function and Are Modulated by Troponin Targeting Agents.
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S-EPMC8431798 | biostudies-literature
UnknownThe cellular and molecular cardiac tissue responses in human inflammatory cardiomyopathies after SARS-CoV-2 infection and COVID-19 vaccination.
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S-EPMC11913730 | biostudies-literature
UnknownSpatial multi-omic map of human myocardial infarction.
Not available
S-EPMC9364862 | biostudies-literature
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