Novel syndromic neurodevelopmental disorder caused by de novo deletion of
Journal
medRxiv : the preprint server for health sciences
Titre abrégé: medRxiv
Pays: United States
ID NLM: 101767986
Informations de publication
Date de publication:
07 Feb 2024
07 Feb 2024
Historique:
medline:
18
3
2024
pubmed:
18
3
2024
entrez:
18
3
2024
Statut:
epublish
Résumé
Genes encoding long non-coding RNAs (lncRNAs) comprise a large fraction of the human genome, yet haploinsufficiency of a lncRNA has not been shown to cause a Mendelian disease.
Identifiants
pubmed: 38496558
doi: 10.1101/2024.01.31.24301497
pmc: PMC10942497
pii:
doi:
Types de publication
Preprint
Langues
eng