Richard, G., Rouan, F., Willoughby, C. E., Brown, N., Chung, P., Ryynänen, M., . . . Russell, L. (2002). Missense Mutations in GJB2 Encoding Connexin-26 Cause the Ectodermal Dysplasia Keratitis-Ichthyosis-Deafness Syndrome. The American Society of Human Genetics.
Citação norma ChicagoRichard, Gabriele, et al. Missense Mutations in GJB2 Encoding Connexin-26 Cause the Ectodermal Dysplasia Keratitis-Ichthyosis-Deafness Syndrome. The American Society of Human Genetics, 2002.
Citação norma MLARichard, Gabriele, et al. Missense Mutations in GJB2 Encoding Connexin-26 Cause the Ectodermal Dysplasia Keratitis-Ichthyosis-Deafness Syndrome. The American Society of Human Genetics, 2002.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.