Walsh, T., Shahin, H., Elkan-Miller, T., Lee, M. K., Thornton, A. M., Roeb, W., . . . Kanaan, M. (2010). Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82. Elsevier.
Citação norma ChicagoWalsh, Tom, et al. Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 As the Cause of Nonsyndromic Hearing Loss DFNB82. Elsevier, 2010.
Citação norma MLAWalsh, Tom, et al. Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 As the Cause of Nonsyndromic Hearing Loss DFNB82. Elsevier, 2010.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.