Eren, E., Edgünlü, T., Asut, E., & Karakaş Çelik, S. (2016). Homozygous Ala65Pro Mutation with V89L Polymorphism in SRD5A2 Deficiency. J Clin Res Pediatr Endocrinol.
Citação norma ChicagoEren, Erdal, Tuba Edgünlü, Emre Asut, and Sevim Karakaş Çelik. "Homozygous Ala65Pro Mutation With V89L Polymorphism in SRD5A2 Deficiency." J Clin Res Pediatr Endocrinol 2016.
MLA citiranjeEren, Erdal, Tuba Edgünlü, Emre Asut, and Sevim Karakaş Çelik. "Homozygous Ala65Pro Mutation With V89L Polymorphism in SRD5A2 Deficiency." J Clin Res Pediatr Endocrinol 2016.
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