Biallelic truncating variants in MAPKAPK5cause a new developmental disorder involving neurological, cardiac, and facial anomalies combined with synpolydactyly

MLA

Horn, Denise, et al. “Biallelic Truncating Variants in MAPKAPK5cause a New Developmental Disorder Involving Neurological, Cardiac, and Facial Anomalies Combined with Synpolydactyly.” Genetics in Medicine, vol. 23, no. 4, Apr. 2021, pp. 679–88. EBSCOhost, https://doi.org/10.1038/s41436-020-01052-2.

APA

Horn, D., Fernández-Núñez, E., Gomez-Carmona, R., Rivera-Barahona, A., Nevado, J., Schwartzmann, S., Ehmke, N., Lapunzina, P., Otaify, G. A., Temtamy, S., Aglan, M., Boschann, F., & Ruiz-Perez, V. L. (2021). Biallelic truncating variants in MAPKAPK5cause a new developmental disorder involving neurological, cardiac, and facial anomalies combined with synpolydactyly. Genetics in Medicine, 23(4), 679–688. https://doi.org/10.1038/s41436-020-01052-2

Chicago

Horn, Denise, Elisa Fernández-Núñez, Ricardo Gomez-Carmona, Ana Rivera-Barahona, Julian Nevado, Sarina Schwartzmann, Nadja Ehmke, et al. 2021. “Biallelic Truncating Variants in MAPKAPK5cause a New Developmental Disorder Involving Neurological, Cardiac, and Facial Anomalies Combined with Synpolydactyly.” Genetics in Medicine 23 (4): 679–88. doi:10.1038/s41436-020-01052-2.