Cite
Genotype-phenotype correlation and description of two novel mutations in Iranian patients with glycogen storage disease 1b (GSD1b)
MLA
Saeed Talebi, et al. “Genotype-Phenotype Correlation and Description of Two Novel Mutations in Iranian Patients with Glycogen Storage Disease 1b (GSD1b).” Orphanet Journal of Rare Diseases, vol. 15, Jan. 2020. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi.dedup.....21f7e4bddde56a9a84dffe43945d8f3c&authtype=sso&custid=ns315887.
APA
Saeed Talebi, Zahra Noroozi, Maryam Eghbali, Ali Rabbani, Mehri Najafi, Fatemeh Yazarlou, Mohammad Hossein Modarressi, Marjan Shakiba, Maryam Abiri, Hosein Alimadadi, & Parastoo Rostami. (2020). Genotype-phenotype correlation and description of two novel mutations in Iranian patients with glycogen storage disease 1b (GSD1b). Orphanet Journal of Rare Diseases, 15.
Chicago
Saeed Talebi, Zahra Noroozi, Maryam Eghbali, Ali Rabbani, Mehri Najafi, Fatemeh Yazarlou, Mohammad Hossein Modarressi, et al. 2020. “Genotype-Phenotype Correlation and Description of Two Novel Mutations in Iranian Patients with Glycogen Storage Disease 1b (GSD1b).” Orphanet Journal of Rare Diseases 15 (January). http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi.dedup.....21f7e4bddde56a9a84dffe43945d8f3c&authtype=sso&custid=ns315887.