Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene.

MLA

Rabionet, Raquel, et al. “Molecular Basis of Childhood Deafness Resulting from Mutations in the GJB2 (Connexin 26) Gene.” Human Genetics, vol. 106, no. 1, Jan. 2000, pp. 40–44. EBSCOhost, https://doi.org/10.1007/s004390051007.

APA

Rabionet, R., Zelante, L., López-Bigas, N., D’Agruma, L., Melchionda, S., Restagno, G., Arbonés, M. L., Gasparini, P., & Estivill, X. (2000). Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene. Human Genetics, 106(1), 40–44. https://doi.org/10.1007/s004390051007

Chicago

Rabionet, Raquel, Leopoldo Zelante, Núria López-Bigas, Leonardo D’Agruma, Salvatore Melchionda, Gabrielle Restagno, Maria Lourdes Arbonés, Paolo Gasparini, and Xavier Estivill. 2000. “Molecular Basis of Childhood Deafness Resulting from Mutations in the GJB2 (Connexin 26) Gene.” Human Genetics 106 (1): 40–44. doi:10.1007/s004390051007.