Kovach, M. J., Lin, J. P., Boyadjiev, S., Campbell, K., Mazzeo, L., Herman, K., . . . Kimonis, V. E. (1999). A unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafness.
Citación estilo ChicagoKovach, M J., et al. A Unique Point Mutation in the PMP22 Gene Is Associated With Charcot-Marie-Tooth Disease and Deafness. 1999.
Cita MLAKovach, M J., et al. A Unique Point Mutation in the PMP22 Gene Is Associated With Charcot-Marie-Tooth Disease and Deafness. 1999.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.