Author

P. Dhandapany

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Open access Jul 2026

AKT1/mTOR/RICTOR risk variants in Indian hypertrophic cardiomyopathy patients

Exome sequencing of an Indian-specific HCM patient cohort was used and six heterozygous missense variants in unrelated patients were identified, highlighting a potential genetic risk associated with the AKT/mTOR/RICTOR axis in patients with HCM.

H. Chittora, D. Notani, P. Dhandapany · medRxiv · 0 citations