Aoyama, Y. Et Al. 2009. Molecular features of 23 patients with glycogen storage disease type III in Turkey: a novel mutation p.R1147G associated with isolated glucosidase deficiency, along with 9 AGL mutations.. Journal of human genetics , vol.54, no.11 , 681-6.

Aoyama, Y., Ozer, I., Demirkol, M., Ebara, T., Murase, T., Podskarbi, T., ... Shin, Y. S.(2009). Molecular features of 23 patients with glycogen storage disease type III in Turkey: a novel mutation p.R1147G associated with isolated glucosidase deficiency, along with 9 AGL mutations.. Journal of human genetics , vol.54, no.11, 681-6.

Aoyama, Yoshiko Et Al. "Molecular features of 23 patients with glycogen storage disease type III in Turkey: a novel mutation p.R1147G associated with isolated glucosidase deficiency, along with 9 AGL mutations.," Journal of human genetics , vol.54, no.11, 681-6, 2009

Aoyama, Yoshiko Et Al. "Molecular features of 23 patients with glycogen storage disease type III in Turkey: a novel mutation p.R1147G associated with isolated glucosidase deficiency, along with 9 AGL mutations.." Journal of human genetics , vol.54, no.11, pp.681-6, 2009

Aoyama, Y. Et Al. (2009) . "Molecular features of 23 patients with glycogen storage disease type III in Turkey: a novel mutation p.R1147G associated with isolated glucosidase deficiency, along with 9 AGL mutations.." Journal of human genetics , vol.54, no.11, pp.681-6.

@article{article, author={Yoshiko Aoyama Et Al. }, title={Molecular features of 23 patients with glycogen storage disease type III in Turkey: a novel mutation p.R1147G associated with isolated glucosidase deficiency, along with 9 AGL mutations.}, journal={Journal of human genetics}, year=2009, pages={681-6} }