Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Darya M. Guseva"'
Autor:
Galina E. Rudenskaya, Varvara A. Kadnikova, Christian Beetz, Tatyana N. Proskokova, Irina G. Sermyagina, Anna A. Stepanova, Valery P. Fedotov, Elena L. Dadaly, Darya M. Guseva, Тatiana V. Markova, Oksana P. Ryzhkova
Publikováno v:
Анналы клинической и экспериментальной неврологии, Vol 14, Iss 1, Pp 44-54 (2020)
Introduction. The autosomal dominant hereditary spastic paraplegia type 3 (SPG3), associated with the ATL1 gene, is a common form of the hereditary spastic paraplegia (HSP). The molecular genetic and clinical features of the SPG3 have not been suffic
Externí odkaz:
https://doaj.org/article/cb785b6c298746ea89b96a7bb419e2f1
Autor:
Yury A. Barbitoff, Mikhail A. Fedyakov, Sorejya A. Urazgildeeva, Natalia A. Semenova, Sergey G. Scherbak, Andrey S. Glotov, V. V. Miroshnikova, Andrey M. Sarana, Victor S. Gurevich, O N Ivanova, Oleg S. Glotov, Olga V. Romanova, A A Panteleeva, Stanislav P. Urazov, Maria V. Muzalevskaya, Inga V. Anisimova, Ekaterina Y. Zakharova, S.N. Pchelina, Darya M. Guseva
Publikováno v:
Biomedical Reports. 14
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 scre
Autor:
Valentina V, Miroshnikova, Olga V, Romanova, Olga N, Ivanova, Mikhail A, Fedyakov, Alexandra A, Panteleeva, Yury A, Barbitoff, Maria V, Muzalevskaya, Sorejya A, Urazgildeeva, Victor S, Gurevich, Stanislav P, Urazov, Sergey G, Scherbak, Andrey M, Sarana, Natalia A, Semenova, Inga V, Anisimova, Darya M, Guseva, Sofya N, Pchelina, Andrey S, Glotov, Ekaterina Y, Zakharova, Oleg S, Glotov
Publikováno v:
Biomedical Reports
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 scre