SCI-E

Durmuş, H., Özoğuz, A., Deymeer, F., Serdaroğlu, P., Aysal, F., Ertaş, M., Günel, M., Başak, N., Parman, Y., “Clinical and Genetic Characteristics of Five Turkish Families with UBQLN2 Mutations”, Neurology, 80, Meeting Abstract: P05078, 2013.

Türkçe

Onat, O.E., Gülsüner, S., Bilguvar, K., Başak, A.N., Topaloğlu, H., Tan, M., Tan, Ü., Günel, M., Özçelik, T., “Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion”, European Journal of Human Genetics 21, 3, 281-285, 2013.

Türkçe

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