APA Alıntı

Leal Esquivel, A., Berghoff, C., Berghoff, M., del Valle Carazo, G., Contreras, C., Montoya, O., . . . Heuss, D. (2003). Charcot-Marie-Tooth disease: A novel Tyr145Ser mutation in the myelin protein zero (MPZ, P0) gene causes different phenotypes in homozygous and heterozygous carriers within one family.

Chicago Stili Alıntı

Leal Esquivel, Alejandro, et al. Charcot-Marie-Tooth Disease: A Novel Tyr145Ser Mutation in the Myelin Protein Zero (MPZ, P0) Gene Causes Different Phenotypes in Homozygous and Heterozygous Carriers Within One Family. 2003.

MLA Alıntı

Leal Esquivel, Alejandro, et al. Charcot-Marie-Tooth Disease: A Novel Tyr145Ser Mutation in the Myelin Protein Zero (MPZ, P0) Gene Causes Different Phenotypes in Homozygous and Heterozygous Carriers Within One Family. 2003.

Uyarı: Bu alıntı herzaman %100 doğru olmayabilir..