Moleküler Biyoloji ve Genetik

Lerche, H., Maljevic, S., Yalçın, Ö., Saltık, S., Çokar, Ö., Aykut-Bingöl, C., Ağan, K., Çağlayan, H., Steinlein, O., Functional Characterization of a Novel Mutation in the S5-H5 Linker of the KCNQ2 K Channel Causing Neonatal Convulsions", Epilepsia 44, Supplement 9, 346, Blackwell Publishing, 2003.

Türkçe

Battaloğlu, E., Poyraz, M., Bissar-Tadmouri, N., Bilir, B., Barış, İ., Deymeer, F., Serdaroğlu, P., Parman: Y., Molecular Basis of Charcot-Marie-Tooth Type 1 (CMT1) Disease in a Cohort of Turkish Patients: European Journal of Human Genetics, 11: Suppl 1, 207, Birmigham, İngiltere. 2003.

Türkçe

Lerche, H., Maljevic, S., Yalçın, Ö., Saltık, S., Çokar, Ö., Aykut-Bingöl, C., Ağan, K., Çağlayan, H., Steinlein, O., Functional Characterization of a Novel Mutation in the S5-H5 Linker of the KCNQ2 K Channel Causing Neonatal Convulsions", Epilepsia 44, Supplement 9, 346, Blackwell Publishing, 2003.

Türkçe

Sayfalar