Schraders, M., Haas, S., Weegerink, N., Oostrik, J., Hu, H., Hoefsloot, L., . . . Kremer, H. (2011). Next-Generation Sequencing Identifies Mutations of SMPX, which Encodes the Small Muscle Protein, X-Linked, as a Cause of Progressive Hearing Impairment. Elsevier.
Citação norma ChicagoSchraders, Margit, et al. Next-Generation Sequencing Identifies Mutations of SMPX, Which Encodes the Small Muscle Protein, X-Linked, As a Cause of Progressive Hearing Impairment. Elsevier, 2011.
Citação norma MLASchraders, Margit, et al. Next-Generation Sequencing Identifies Mutations of SMPX, Which Encodes the Small Muscle Protein, X-Linked, As a Cause of Progressive Hearing Impairment. Elsevier, 2011.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.