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Molecular Mechanisms of Inherited Cardiomyopathies and Arrhythmias

Home Research projects using our data Molecular Mechanisms of Inherited…

Primary organisation: Victor Chang Cardiac Research Institute (VCCRI)

Principal Investigator: Professor Diane Fatkin

Flagship requested: Cardiovascular genetic disorders

Co-applicants: Dr Renee Johnson (VCCRI), A/Professor Elani Giannoulatou (VCCRI), Dr Emma Rath (VCCRI), Dr Paul Young (VCCRI), Magdalena Soka (VCCRI), Monique Ohanian (VCCRI)

Approval date: March 2022

Applicant’s project summary:

Our project aims to identify genetic causes of the heart muscle condition, dilated cardiomyopathy (DCM). Currently, more than half of people with DCM undergoing genetic testing do not have a genetic result identified. The projects we are proposing aim to improve the detection and understanding of genetic results for patients.


More projects

Accelerated gene identification for families with rare genetic disorders

Genomic diagnosis and gene discovery in rare disease via analysis of existing samples and datasets

The Australian Undiagnosed Diseases Network (UDN-Aus): An internationally networked national approach for transforming diagnosis for individuals living with rare diseases

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