Polfus, L. M., Boerwinkle, E., Gibbs, R. A., Metcalf, G., Muzny, D., Veeraraghavan, N., . . . Gupta-Malhotra, M. (2016). Whole-exome sequencing reveals an inherited R566X mutation of the epithelial sodium channel β-subunit in a case of early-onset phenotype of Liddle syndrome. Cold Spring Harb Mol Case Stud.
Citação norma ChicagoPolfus, Linda M., et al. "Whole-exome Sequencing Reveals an Inherited R566X Mutation of the Epithelial Sodium Channel β-subunit in a Case of Early-onset Phenotype of Liddle Syndrome." Cold Spring Harb Mol Case Stud 2016.
Citação norma MLAPolfus, Linda M., et al. "Whole-exome Sequencing Reveals an Inherited R566X Mutation of the Epithelial Sodium Channel β-subunit in a Case of Early-onset Phenotype of Liddle Syndrome." Cold Spring Harb Mol Case Stud 2016.