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Carlos Chellaram

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Open access 2026

Familial Characterization of the DSC2 c.354+1G>T Splice-Site Variant Cardiac Disease

The findings support genetic counseling, cascade testing, and cardiovascular surveillance, however, the current clinical and segregation data do not establish definitive causality for hypertrophic cardiomyopathy or conduction disease.

JoseCedeno, Carlos Chellaram, Carolina Vega et al. · 0 citations

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