Phenotypic variability and modifier variants in children with hereditary heart diseases
Despite the recent achievements in searching for the causes of monogenic human diseases, there is still a massive gap in understanding the molecular causes of phenotypic variability. At the moment, it is evident that the pathogenic genetic variant often acts together with the other genetic and non-g...
Main Authors: | N. V. Shcherbakova, A. B. Zhironkina, V. Yu. Voinova, R. A. Ildarova, M. A. Shkolnikova |
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Format: | Article |
Language: | Russian |
Published: |
Ltd. “The National Academy of Pediatric Science and Innovation”
2021-07-01
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Series: | Rossijskij Vestnik Perinatologii i Pediatrii |
Subjects: | |
Online Access: | https://www.ped-perinatology.ru/jour/article/view/1400 |
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