Variants in
PHF8
X-linked intellectual disability
epigenetic gene regulation
histone demethylation
orofacial clefting
Journal
HGG advances
ISSN: 2666-2477
Titre abrégé: HGG Adv
Pays: United States
ID NLM: 101772885
Informations de publication
Date de publication:
14 Jul 2022
14 Jul 2022
Historique:
received:
14
12
2021
accepted:
18
03
2022
entrez:
26
4
2022
pubmed:
27
4
2022
medline:
27
4
2022
Statut:
epublish
Résumé
Loss-of-function variants in
Identifiants
pubmed: 35469323
doi: 10.1016/j.xhgg.2022.100102
pii: S2666-2477(22)00018-5
pmc: PMC9034099
doi:
Types de publication
Journal Article
Langues
eng
Pagination
100102Subventions
Organisme : NIGMS NIH HHS
ID : T32 GM008638
Pays : United States
Organisme : NICHD NIH HHS
ID : P50 HD105354
Pays : United States
Organisme : NHGRI NIH HHS
ID : U01 HG011744
Pays : United States
Organisme : NHGRI NIH HHS
ID : UM1 HG006493
Pays : United States
Organisme : NHGRI NIH HHS
ID : U24 HG008956
Pays : United States
Organisme : NIH HHS
ID : S10 OD021553
Pays : United States
Organisme : Wellcome Trust
Pays : United Kingdom
Commentaires et corrections
Type : ErratumIn
Informations de copyright
© 2022 The Author(s).
Déclaration de conflit d'intérêts
J.J., J.Z., A.T., R.P., and K.M. are employees of GeneDx, Inc. All other authors have no conflict of interest to declare.
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