Identification of novel variants in the LDLR gene in Russian patients with familial hypercholesterolemia using targeted sequencing

Familial hypercholesterolemia (FH) is caused by mutations in various genes, including the LDLR, APOB and PSCK9 genes; however, the spectrum of these mutations in Russian individuals has not been fully investigated. In the present study, mutation screening was performed on the LDLR gene and other FH-...

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שמור ב:
מידע ביבליוגרפי
הוצא לאור ב:Biomed Rep
Main Authors: Miroshnikova, Valentina V., Romanova, Olga V., Ivanova, Olga N., Fedyakov, Mikhail A., Panteleeva, Alexandra A., Barbitoff, Yury A., Muzalevskaya, Maria V., Urazgildeeva, Sorejya A., Gurevich, Victor S., Urazov, Stanislav P., Scherbak, Sergey G., Sarana, Andrey M., Semenova, Natalia A., Anisimova, Inga V., Guseva, Darya M., Pchelina, Sofya N., Glotov, Andrey S., Zakharova, Ekaterina Y., Glotov, Oleg S.
פורמט: Artigo
שפה:Inglês
יצא לאור: D.A. Spandidos 2021
נושאים:
Articles
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC7694592/
https://ncbi.nlm.nih.gov/pubmed/33269076
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/br.2020.1391
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