Familial Hypertrophic Cardiomyopathy Latest Advances
Find the Latest Research About Familial Hypertrophic Cardiomyopathy
Last Updated: 09/19/2026
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Found 1094 publications
Whole-exome sequencing identifies rare genetic variants in Egyptian patients with hypertrophic cardiomyopathy: a pilot study.
Journal: Cardiology in the young
Published: July 21, 2026
Cas13-Mediated RNA Base Editing for the Treatment of Hereditary Hypertrophic Cardiomyopathy.
Journal: Circulation
Published: May 18, 2026
Hypertrophic Cardiomyopathy in the Genomic Era: Genetic Testing Is No Longer Optional.
Journal: JACC. Heart failure
Published: May 17, 2026
Genetic Testing in Hypertrophic Cardiomyopathy: Expanding Global Representation While Refining Interpretation.
Journal: Arquivos brasileiros de cardiologia
Published: May 15, 2026
Therapeutic potential of ELABELA in alleviating hereditary hypertrophic cardiomyopathy.
Journal: Journal of advanced research
Published: March 25, 2026
Novel GLA variant (c.752A>C; p.Glu251Ala) identified in a patient with Fabry cardiomyopathy and familial segregation.
Journal: Frontiers in molecular biosciences
Published: March 12, 2026
Impact of variant reclassification on genetic testing yield and clinical outlook in patients with hypertrophic cardiomyopathy.
Journal: International journal of cardiology
Published: March 11, 2026
Hereditary Hemochromatosis and Hypertrophic Cardiomyopathy as Tier 1 Genomic Conditions: Implications for Adult Population Genomic Screening.
Journal: Public health genomics
Published: March 06, 2026
Case Report: Homozygous mutation in the ACAD9 gene revealed in a pediatric patient initially diagnosed with familial cardiac hypertrophy.
Journal: Frontiers in medicine
Published: March 06, 2026
Epi-Allele elicits compensatory expression of the non-targeted allele and prevents haploinsufficiency in dominant genetic diseases.
Journal: Cell stem cell
Published: February 25, 2026
Last Updated: 09/19/2026