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Wahidullah Mansoor

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Aug 2026

Molecular Characterization of two NR2F2 Exons identifies a Rare Intronic Variant Enriched in Indonesian Congenital Heart Disease Patients

It is suggested that pathogenic coding variants within these exons are unlikely to be a frequent genetic cause of CHD in Indonesian patients, and this study highlights the need for population-specific genetic investigations and their contribution to human cardiac development.

Wahidullah Mansoor · 0 citations

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