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G. Kh. Bagyeva
G. Kh. Bagyeva
Academy of Medical Sciences, United Kingdom
Genetics
Parkinson's disease
Dominance (genetics)
Parkin
LRRK2
3
Papers
21
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Гетерогенность спорадической болезни Паркинсона: молекулярный подход к решению проблемы
2017
S. N. Illarioshkin
P. A. Slominsky
M. I. Shadrina
G. Kh. Bagyeva
T. B. Zagorovskaya
Markova Ed
A.V. Karabanov
Poleshchuk Vv
E. V. Polevaya
N. Fedorova
S. A. Limborskaya
Irina A. Ivanova-Smolenskaya
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Analysis of the α-synuclein gene dosage variation associated with autosomal dominant form of Parkinson’s disease
2009
Russian Journal of Genetics
E. V. Semenova
M. I. Shadrina
P. A. Slominsky
S. N. Illarioshkin
G. Kh. Bagyeva
A.V. Karabanov
I. A. Ivanova-Smolenskaia
S. A. Limborska
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A common leucine-rich repeat kinase 2 gene mutation in familial and sporadic Parkinson's disease in Russia
2007
European Journal of Neurology
S. N. Illarioshkin
Maria I. Shadrina
Petr Slominsky
E. V. Bespalova
T. B. Zagorovskaya
G. Kh. Bagyeva
Markova Ed
S. A. Limborska
Irina A. Ivanova-Smolenskaya
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Citations (21)
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