APA aipamena

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 Style aipamena

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 aipamena

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.