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[Molecular basis of Parkinson's disease linked with mutations in the LRRK2 gene].
Mol Biol (Mosk). 2014 Jan-Feb;48(1):3-14.
Mol Biol (Mosk). 2014.
PMID: 25842821
Free article.
Review.
Russian.
[Clinical features of LRRK2-associated Parkinson's disease].
Pchelina SN, Ivanova ON, Emel'ianov AK, Iakimovskiĭ AF.
Pchelina SN, et al. Among authors: emel ianov ak.
Zh Nevrol Psikhiatr Im S S Korsakova. 2011;111(12):56-62.
Zh Nevrol Psikhiatr Im S S Korsakova. 2011.
PMID: 22433811
Russian.
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[Apoptosis of peripheral blood lymphocytes in patients with LRRK2-assoctated Parkinson's disease].
Usenko TS, Emel'ianov AK, Iakimovskiĭ AF, Bogan'kova NA, Vavilova TV, Shvartsman AL, Pchelina SN.
Usenko TS, et al. Among authors: emel ianov ak.
Tsitologiia. 2012;54(1):44-8.
Tsitologiia. 2012.
PMID: 22567899
Russian.
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G2019S LRRK2 mutation in familial and sporadic Parkinson's disease in Russia.
Pchelina SN, Yakimovskii AF, Ivanova ON, Emelianov AK, Zakharchuk AH, Schwarzman AL.
Pchelina SN, et al.
Mov Disord. 2006 Dec;21(12):2234-6. doi: 10.1002/mds.21134.
Mov Disord. 2006.
PMID: 17044089
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