Beyzaei, Z. Et Al. 2021. Novel mutations in the PHKB gene in an iranian girl with severe liver involvement and glycogen storage disease type IX: a case report and review of literature.. BMC pediatrics , vol.21, no.1 , 175.

Beyzaei, Z., Ezgu, F. S., Geramizadeh, B., Alborzi, A., & Shojazadeh, A., (2021). Novel mutations in the PHKB gene in an iranian girl with severe liver involvement and glycogen storage disease type IX: a case report and review of literature.. BMC pediatrics , vol.21, no.1, 175.

Beyzaei, Zahra Et Al. "Novel mutations in the PHKB gene in an iranian girl with severe liver involvement and glycogen storage disease type IX: a case report and review of literature.," BMC pediatrics , vol.21, no.1, 175, 2021

Beyzaei, Zahra Et Al. "Novel mutations in the PHKB gene in an iranian girl with severe liver involvement and glycogen storage disease type IX: a case report and review of literature.." BMC pediatrics , vol.21, no.1, pp.175, 2021

Beyzaei, Z. Et Al. (2021) . "Novel mutations in the PHKB gene in an iranian girl with severe liver involvement and glycogen storage disease type IX: a case report and review of literature.." BMC pediatrics , vol.21, no.1, p.175.

@article{article, author={Zahra Beyzaei Et Al. }, title={Novel mutations in the PHKB gene in an iranian girl with severe liver involvement and glycogen storage disease type IX: a case report and review of literature.}, journal={BMC pediatrics}, year=2021, pages={175} }