Comment
doi: 10.1016/j.gim.2021.11.007.
Epub 2021 Dec 6.
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
Affiliations
- PMID: 34906509
- DOI: 10.1016/j.gim.2021.11.007
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Comment
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
Genet Med.
2022 Mar.
Free article
No abstract available
Conflict of interest statement
Conflict of Interest The authors declare no conflicts of interest.
Comment in
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Response to Cueto-González et al.Genet Med. 2022 Mar;24(3):757. doi: 10.1016/j.gim.2021.11.006. Epub 2021 Dec 7. Genet Med. 2022. PMID: 34906511 No abstract available.
Comment on
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Loss-of-function and missense variants in NSD2 cause decreased methylation activity and are associated with a distinct developmental phenotype.Genet Med. 2021 Aug;23(8):1474-1483. doi: 10.1038/s41436-021-01158-1. Epub 2021 May 3. Genet Med. 2021. PMID: 33941880 Free PMC article.
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