Genetic bases and phenotypes of autosomal recessive Parkinson disease in a Turkish population

Tarih
2012
Yazar
Dogu, O.
BRICE, A.
LESAGE, S.
Lohmann, E.
Sevinc, G.
Emre, M.
Dursun, B.
Yazici, J.
Babacan, G.
Erginel-Unaltuna, Nihan
Gurvit, H.
Hanagasi, Haşmet Ayhan
Bilgic, B.
HONORE, A.
Kaleagasi, H.
Üst veri
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Özet
Background and purpose: To evaluate the phenotype and the frequencies of mutations in PRKN, DJ1 and PINK1 genes in patients with Parkinson disease (PD) in Turkey.
Bağlantı
http://hdl.handle.net/20.500.12627/22615
https://doi.org/10.1111/j.1468-1331.2011.03639.x
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