Loss-of-function and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct developmental phenotype

MLA

Newell Belnap, et al. “Loss-of-Function and Missense Variants in NSD2 Cause Decreased Methylation Activity and Are Associated with a Distinct Developmental Phenotype.” Genetics in Medicine, vol. 23, Aug. 2021, pp. 1474–83. EBSCOhost, https://doi.org/10.1038/s41436-021-01158-1.

APA

Newell Belnap, Bert B.A. de Vries, Austin Larson, Rolph Pfundt, Marijke R. Wevers, Valérie Benoit, Markus Zweier, Pascal Joset, Anita Rauch, Angela Bahr, Jeroen Mourmans, Patricia G Wheeler, Or Gozani, Marisa V. Andrews, Monica H. Wojcik, Didier Lacombe, Sarah Grotto, Marwan Shinawi, Lot Snijders Blok, … Vassilis Tsatsaris. (2021). Loss-of-function and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct developmental phenotype. Genetics in Medicine, 23, 1474–1483. https://doi.org/10.1038/s41436-021-01158-1

Chicago

Newell Belnap, Bert B.A. de Vries, Austin Larson, Rolph Pfundt, Marijke R. Wevers, Valérie Benoit, Markus Zweier, et al. 2021. “Loss-of-Function and Missense Variants in NSD2 Cause Decreased Methylation Activity and Are Associated with a Distinct Developmental Phenotype.” Genetics in Medicine 23 (August): 1474–83. doi:10.1038/s41436-021-01158-1.