Moleküler Biyoloji ve Genetik

Lohmann, E., Köroğlu, C., Hanağası, H.A., Dursun, B., Taşan, E., Tolun, A., “A homozygous frameshift mutation of sepiapterin reductase gene causing parkinsonism with onset in childhood”, Parkinsonism & Related Disorders, 18, 2, 191-193, 2012.

Türkçe

Lahut, S., Omur, O., Uyan, O., Ağım, Z.S., Özoğuz, A., Parman, Y., Deymeer, F., Oflazer, P., Koç, F., Özcelik, H., Auburger, G., Başak, A.N., “ATXN2 and its neighbouring gene SH2B3 are associated with increased ALS risk in the Turkish population”, Plos One, 7, 8, Article Number: e42956, 2012.

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