Searching for new genes associated with the familial hypercholesterolemia phenotype using whole-genome sequencing and machine learning

One of the most common congenital metabolic disorders is familial hypercholesterolemia. Familial hypercholesterolemia is a condition caused by a type of genetic defect leading to a decreased rate of removal of low-density lipoproteins from the bloodstream and a pronounced increase in the blood level...

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Detalles Bibliográficos
Autores principales: Ivanoshchuk, D.E., Kolker, A.B., Timoshchenko, O.V., Semaev, S.E., Shakhtshneider, E.V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Federal Research Center Institute of Cytology and Genetics of Siberian Branch of the Russian Academy of Sciences 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10551936/
https://www.ncbi.nlm.nih.gov/pubmed/37808210
http://dx.doi.org/10.18699/VJGB-23-63

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10551936/
https://www.ncbi.nlm.nih.gov/pubmed/37808210
http://dx.doi.org/10.18699/VJGB-23-63

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