American scientists, led by Peter Munch, published the results of their research.

This discovery can become a rescue for patients with Brugada syndrome.

The disease itself can cause a sudden death from arrhythmia due to genetic abnormalities in the functioning of the heart.

The reason for this was the gene SCN5A, but experts also suggested that their studies can not be called complete and subject to rigorous tests. Scientists have to do more than one test to make sure their work is correct.

They also came to the conclusion that during the work it would be expedient to create a single database where information is brought about all the genes being studied in the course of treatment.

This will greatly facilitate the treatment of all patients because of the rapid available to the right information.

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