Editorial for the Fragile X Syndrome Genetics Special Issue: May 2023.


Journal

Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097

Informations de publication

Date de publication:
25 05 2023
Historique:
received: 15 05 2023
accepted: 23 05 2023
medline: 29 6 2023
pubmed: 28 6 2023
entrez: 28 6 2023
Statut: epublish

Résumé

Fragile X syndrome (FXS) is the leading single-gene cause of inherited intellectual disability and autism [...].

Identifiants

pubmed: 37372328
pii: genes14061148
doi: 10.3390/genes14061148
pmc: PMC10297929
pii:
doi:

Types de publication

Editorial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Références

Genes (Basel). 2022 Jan 30;13(2):
pubmed: 35205326
Genes (Basel). 2023 Feb 16;14(2):
pubmed: 36833432
Genes (Basel). 2021 Sep 26;12(10):
pubmed: 34680911
Genes (Basel). 2021 Nov 27;12(12):
pubmed: 34946857
Genes (Basel). 2022 Sep 15;13(9):
pubmed: 36140821
Genes (Basel). 2021 Oct 17;12(10):
pubmed: 34681027
Genes (Basel). 2021 Oct 22;12(11):
pubmed: 34828275
Genes (Basel). 2022 Sep 08;13(9):
pubmed: 36140775
Genes (Basel). 2022 Aug 30;13(9):
pubmed: 36140728
Genes (Basel). 2021 May 24;12(6):
pubmed: 34073864
Genes (Basel). 2022 Sep 16;13(9):
pubmed: 36140827

Auteurs

David E Godler (DE)

Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, VIC 3052, Australia.
Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, VIC 3052, Australia.

William T Brown (WT)

Central Clinical School, Sydney Medical School, University of Sydney, Camperdown, NSW 2006, Australia.
Institute for Basic Research in Developmental Disabilities, Staten Island, NY 10314, USA.

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Classifications MeSH