Toplantı Özeti

Maljevic, S., Naros, G., Yalçın, O., Dervent, A., Saltık, S., Çokar, O., Aykut-Bingo, C., Ağan, K., Çağlayan, H., Steinlein, O.K., Lerchel, H., “A BFNC Mutation in the S5-h5 Linker of the kv7.2 Channel Reduces M Currents and Exhibits a Dominant Negative Effect”, Biophysical Journal, 111A-111A, 2007.

Türkçe

Çiftçi, E.D., Poyraz, M., Eraksoy, M., Direskeneli, G.S., Halefoğlu, A., Battaloğlu, E., Serdaroğlu, P., Deymeer, F., Parman, Y., “X-Linked Charcot-Marie-Tooth Disease and Relapsing-Remitting Multiple Sclerosis: Is It a Coincidence or an Aetiopathogenetic Relationship?”, Journal of Neurology, 253, 10-10, 2006.

Türkçe

Çörüt, A., Şenyiğit, A., Uğur, S.A., Altın, S., Özçelik, U., Çalışır, H., Yıldırım, Z., Göçmen, A., Tolun, A., “Mutations in a Solute Carrier Gene are Responsible for Pulmonary Alveolar and Partly for Testicular Microlithiasis”, FEBS Journal, 273, 233-233, 2006.

Türkçe

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