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Article

Sex hormone receptor gene variation associated with phenotype in male hypertrophic cardiomyopathy patients.

Journal of molecular and cellular cardiology - 1 Aug 2008

Lind Joanne M, Chiu Christine, Ingles Jodie, Yeates Laura, Humphries Stephen E, Heather Alison K, Semsarian Christopher

Abstract excerpt

Hypertrophic cardiomyopathy (HCM) is a clinically heterogeneous disease, which suggests that a number of factors exist which modify disease outcome. Gender may be one such factor as more males present with the disease compared with females. The aim of the present study was to determine if an association exists between genetic variation in sex hormone receptors and the development of left ventricular hypertrophy...

Read the complete abstract on PubMed

Topics

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Share to Cardiomyopathy, Hypertrophic
Share to Estrogen Receptor alpha

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Variation

Share to Gonadal Steroid Hormones

Share to Hypertrophy, Left Ventricular

Share to Polymorphism, Single Nucleotide

Share to Promoter Regions, Genetic

Share to Receptors, Androgen

Source

Identifiers

PMID: 18617186
DOI: 10.1016/j.yjmcc.2008.05.016

Genes

ESR1
ESR2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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