Correspondence on "Loss-of-function and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct developmental phenotype" by Zanoni et al.
Overview publication
| Title | Correspondence on "Loss-of-function and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct developmental phenotype" by Zanoni et al. |
| Date | 2022-03-01 |
| Issue name | Genetics in medicine : official journal of the American College of Medical Genetics |
| Issue number | v24.3:754-756 |
| DOI | 10.1016/j.gim.2021.11.007 |
| PubMed | 34906509 |
| Authors | |
| Read | Read publication |