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LONDON, Aug. 2 (Xinhua) -- A team of researchers has successfully corrected a disease-causing gene mutation in human embryos by using a gene-editing tool, stopping it from passing to future generations, according to a study published Wednesday in the journal Nature.


The new method uses the gene-editing tool CRISPR to target a mutation in nuclear DNA that causes hypertrophic cardiomyopathy, a common genetic heart disease condition which can cause sudden cardiac death and heart failure.


Hypertrophic cardiomyopathy affects an estimated one in 500 people and can lead to heart failure and sudden death.