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;24(3):754-756.
doi: 10.1016/j.gim.2021.11.007.
Epub 2021 Dec 6.
1 Department of Clinical and Molecular Genetics, Vall d'Hebron Barcelona Campus Hospital, Barcelona, Spain; Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Vall d'Hebron Barcelona Campus Hospital, Autonomous University of Barcelona, Barcelona, Spain; European Reference Network Craniofacial Anomalies and ENT disorders (ERN CRANIO) and ERN ITHACA, Barcelona, Spain. Electronic address: amcueto@vhebron.net.
2 Department of Clinical and Molecular Genetics, Vall d'Hebron Barcelona Campus Hospital, Barcelona, Spain; Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Vall d'Hebron Barcelona Campus Hospital, Autonomous University of Barcelona, Barcelona, Spain.
3 Department of Clinical and Molecular Genetics, Vall d'Hebron Barcelona Campus Hospital, Barcelona, Spain; Medicine Genetics Group, Vall d'Hebron Research Institute (VHIR), Vall d'Hebron Barcelona Campus Hospital, Autonomous University of Barcelona, Barcelona, Spain; European Reference Network Craniofacial Anomalies and ENT disorders (ERN CRANIO) and ERN ITHACA, Barcelona, Spain.