Moleküler Biyoloji ve Genetik

Özkınay, F., Pehlivan, S., Onay, H., Van, D.E.N., Vardar, F., Koturoğlu, G., Aksu, G., Ünal, D., Tekgül, H., Can, S., Özkınay, C., “Purine Nucleoside Phosphorylase Deficiency in a Patient with Spastic Paraplegia and Recurrent Infections”, Journal of Child Neurology, 22, 6, 741-743, 2007.

Türkçe

Stendel, C., Roos, A., Deconinck, T., , Battaloğlu, E., et al., “Peripheral Nerve Demyelination Caused by a Mutant Rho GTPase Guanine Nucleotide Exchange Factor, Frabin/FGD4”, American Journal of Human Genetics, 81, 1, 158-164, 2007.

Türkçe

Yalçın, O., Çağlayan, S.H., Saltık, S., Çokar, O., Ağan, K., Dervent, A., Steinlein, O.K., “A Novel Missense Mutation (N258S) in the KCNQ2 Gene in a Turkish Family Afflicted with Benign Familial Neonatal Convulsions (BFNC)”, Turkish Journal of Pediatrics, 49, 4, 385-389, 2007.

Türkçe

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

Sayfalar