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Article

Genetic Insights from Consanguineous Cardiomyopathy Families.

Genes - 10 Jan 2023

Maurer Constance, Boleti Olga, Najarzadeh Torbati Paria, Norouzi Farzaneh, Fowler Anna Nicole Rebekah, Minaee Shima, Salih Khalid Hama, Taherpour Mehdi, Birjandi Hassan, Alizadeh Behzad, Salih Aso Faeq, Bijari Moniba, Houlden Henry, Pittman Alan Michael, Maroofian Reza, Almashham Yahya H, Karimiani Ehsan Ghayoor, Kaski Juan Pablo, Faqeih Eissa Ali, Vakilian Farveh, Jamshidi Yalda

Abstract excerpt

Inherited cardiomyopathies are a prevalent cause of heart failure and sudden cardiac death. Both hypertrophic (HCM) and dilated cardiomyopathy (DCM) are genetically heterogeneous and typically present with an autosomal dominant mode of transmission. Whole exome sequencing and autozygosity mapping was carried out in eight un-related probands from consanguineous Middle Eastern families presenting with HCM/DCM...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 36672924
DOI: 10.3390/genes14010182
PMCID: PMC9858866

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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