Mono-allelic loss of YTHDF3 and neurodevelopmental disorder: clinical features of four individuals with 8q12.3 deletions.
YTHDF3 protein
chromosome deletion
developmental delay
heterozygote
human
intellectual disability
Journal
Clinical genetics
ISSN: 1399-0004
Titre abrégé: Clin Genet
Pays: Denmark
ID NLM: 0253664
Informations de publication
Date de publication:
02 2022
02 2022
Historique:
revised:
08
10
2021
received:
07
09
2021
accepted:
25
10
2021
pubmed:
29
10
2021
medline:
29
3
2022
entrez:
28
10
2021
Statut:
ppublish
Résumé
The YTH domain family member 3 gene (YTHDF3) encodes a reader of the abundant N6-methyladenosine (m
Substances chimiques
RNA-Binding Proteins
0
YTHDF3 protein, human
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
208-213Subventions
Organisme : Aarhus University
Organisme : Region of Southern Denmark
Organisme : Wellcome Trust
Pays : United Kingdom
Informations de copyright
© 2021 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
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