A. AYAZ Et Al. , "Interacting with AP1 complex mutated synergin gamma (SYNRG) reveals a novel coatopathy in the form of complicated hereditary spastic paraplegia," Brain and Development , vol.44, no.5, pp.329-335, 2022
AYAZ, A. Et Al. 2022. Interacting with AP1 complex mutated synergin gamma (SYNRG) reveals a novel coatopathy in the form of complicated hereditary spastic paraplegia. Brain and Development , vol.44, no.5 , 329-335.
AYAZ, A., Uzunhan, T. A., & AYDIN, K., (2022). Interacting with AP1 complex mutated synergin gamma (SYNRG) reveals a novel coatopathy in the form of complicated hereditary spastic paraplegia. Brain and Development , vol.44, no.5, 329-335.
AYAZ, Akif, Tugce Aksu Uzunhan, And Kürşad AYDIN. "Interacting with AP1 complex mutated synergin gamma (SYNRG) reveals a novel coatopathy in the form of complicated hereditary spastic paraplegia," Brain and Development , vol.44, no.5, 329-335, 2022
AYAZ, Akif Et Al. "Interacting with AP1 complex mutated synergin gamma (SYNRG) reveals a novel coatopathy in the form of complicated hereditary spastic paraplegia." Brain and Development , vol.44, no.5, pp.329-335, 2022
AYAZ, A. Uzunhan, T. A. And AYDIN, K. (2022) . "Interacting with AP1 complex mutated synergin gamma (SYNRG) reveals a novel coatopathy in the form of complicated hereditary spastic paraplegia." Brain and Development , vol.44, no.5, pp.329-335.
@article{article, author={Akif AYAZ Et Al. }, title={Interacting with AP1 complex mutated synergin gamma (SYNRG) reveals a novel coatopathy in the form of complicated hereditary spastic paraplegia}, journal={Brain and Development}, year=2022, pages={329-335} }