SHP2's gain-of-function in Werner syndrome causes childhood disease onset likely resulting from negative genetic interaction.

MLA

Priolo, Manuela, et al. “SHP2’s Gain-of-Function in Werner Syndrome Causes Childhood Disease Onset Likely Resulting from Negative Genetic Interaction.” Clinical Genetics, vol. 102, no. 1, July 2022, pp. 12–21. EBSCOhost, https://doi.org/10.1111/cge.14140.

APA

Priolo, M., Palermo, V., Aiello, F., Ciolfi, A., Pannone, L., Muto, V., Motta, M., Mancini, C., Radio, F. C., Niceta, M., Leoni, C., Pintomalli, L., Carrozzo, R., Rajola, G., Mammì, C., Zampino, G., Martinelli, S., Dallapiccola, B., Pichierri, P., & Tartaglia, M. (2022). SHP2’s gain-of-function in Werner syndrome causes childhood disease onset likely resulting from negative genetic interaction. Clinical Genetics, 102(1), 12–21. https://doi.org/10.1111/cge.14140

Chicago

Priolo, Manuela, Valentina Palermo, Francesca Aiello, Andrea Ciolfi, Luca Pannone, Valentina Muto, Marialetizia Motta, et al. 2022. “SHP2’s Gain-of-Function in Werner Syndrome Causes Childhood Disease Onset Likely Resulting from Negative Genetic Interaction.” Clinical Genetics 102 (1): 12–21. doi:10.1111/cge.14140.