<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(23)</volume><submitter>Tran DD</submitter><pubmed_abstract>&lt;b>Background&lt;/b>: Cardiomyopathy, including dilated cardiomyopathy (DCM) and hypertrophic cardiomyopathy (HCM), is a major cause of heart failure (HF) and a leading indication for heart transplantation. Of these patients, 20-50% have a genetic cause, so understanding the genetic basis of cardiomyopathy will provide knowledge about the pathogenesis of the disease for diagnosis, treatment, prevention, and genetic counseling for families. &lt;b>Methods&lt;/b>: This study collected nine patients from different Vietnamese families for genetic analysis at The Cardiovascular Center, E Hospital, Hanoi, Vietnam. The patients were diagnosed with cardiomyopathy based on clinical symptoms. Whole-exome sequencing (WES) was performed in the Vietnamese patients to identify variants associated with cardiomyopa</pubmed_abstract><journal>Diagnostics (Basel, Switzerland)</journal><pagination>2709</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11640685</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Three Novel Pathogenic Variants in Unrelated Vietnamese Patients with Cardiomyopathy.</pubmed_title><pmcid>PMC11640685</pmcid><pubmed_authors>Oanh TTK</pubmed_authors><pubmed_authors>Tung NV</pubmed_authors><pubmed_authors>Tien DA</pubmed_authors><pubmed_authors>Huy BQ</pubmed_authors><pubmed_authors>Tran DD</pubmed_authors><pubmed_authors>Duc NM</pubmed_authors><pubmed_authors>Hoang NH</pubmed_authors><pubmed_authors>Huu NC</pubmed_authors><pubmed_authors>Lien NTP</pubmed_authors><pubmed_authors>Thanh LT</pubmed_authors><pubmed_authors>Hien NT</pubmed_authors><pubmed_authors>Lien NTK</pubmed_authors><pubmed_authors>Nguyen PT</pubmed_authors><pubmed_authors>Thu DTH</pubmed_authors><pubmed_authors>Lan NN</pubmed_authors></additional><is_claimable>false</is_claimable><name>Three Novel Pathogenic Variants in Unrelated Vietnamese Patients with Cardiomyopathy.</name><description>&lt;b>Background&lt;/b>: Cardiomyopathy, including dilated cardiomyopathy (DCM) and hypertrophic cardiomyopathy (HCM), is a major cause of heart failure (HF) and a leading indication for heart transplantation. Of these patients, 20-50% have a genetic cause, so understanding the genetic basis of cardiomyopathy will provide knowledge about the pathogenesis of the disease for diagnosis, treatment, prevention, and genetic counseling for families. &lt;b>Methods&lt;/b>: This study collected nine patients from different Vietnamese families for genetic analysis at The Cardiovascular Center, E Hospital, Hanoi, Vietnam. The patients were diagnosed with cardiomyopathy based on clinical symptoms. Whole-exome sequencing (WES) was performed in the Vietnamese patients to identify variants associated with cardiomyopa</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2026-05-26T20:09:55.433Z</modification><creation>2025-04-06T22:30:07.658Z</creation></dates><accession>S-EPMC11640685</accession><cross_references><pubmed>39682617</pubmed><doi>10.3390/diagnostics14232709</doi></cross_references></HashMap>