Cite
Missense variants in the Arg206 residue of HNRNPH2: Further evidence of causality and expansion of the phenotype.
MLA
Peron, Angela, et al. “Missense Variants in the Arg206 Residue of HNRNPH2: Further Evidence of Causality and Expansion of the Phenotype.” American Journal of Medical Genetics. Part A, vol. 182, no. 4, Apr. 2020, pp. 823–28. EBSCOhost, https://doi.org/10.1002/ajmg.a.61486.
APA
Peron, A., Novara, F., La Briola, F., Merati, E., Giannusa, E., Segalini, E., Anniballi, G., Vignoli, A., Ciccone, R., & Canevini, M. P. (2020). Missense variants in the Arg206 residue of HNRNPH2: Further evidence of causality and expansion of the phenotype. American Journal of Medical Genetics. Part A, 182(4), 823–828. https://doi.org/10.1002/ajmg.a.61486
Chicago
Peron, Angela, Francesca Novara, Francesca La Briola, Elisabetta Merati, Emanuela Giannusa, Elena Segalini, Gloria Anniballi, Aglaia Vignoli, Roberto Ciccone, and Maria Paola Canevini. 2020. “Missense Variants in the Arg206 Residue of HNRNPH2: Further Evidence of Causality and Expansion of the Phenotype.” American Journal of Medical Genetics. Part A 182 (4): 823–28. doi:10.1002/ajmg.a.61486.