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

David E Godler; William T Brown

doi:10.3390/genes14061148

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

Genes (Basel). 2023 May 25;14(6):1148. doi: 10.3390/genes14061148.

Authors

David E Godler^{1

2}, William T Brown^{3

4}

Affiliations

¹ Diagnosis and Development, Murdoch Children's Research Institute, Royal Children's Hospital, Melbourne, VIC 3052, Australia.
² Department of Paediatrics, Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, Parkville, VIC 3052, Australia.
³ Central Clinical School, Sydney Medical School, University of Sydney, Camperdown, NSW 2006, Australia.
⁴ Institute for Basic Research in Developmental Disabilities, Staten Island, NY 10314, USA.

Abstract

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

Publication types

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

MeSH terms

Autistic Disorder* / genetics
Fragile X Syndrome* / genetics
Humans
Intellectual Disability* / genetics

Grants and funding

DEG salary has been supported by National Health and Medical Research Council, Australia grants [No 1017263, 104299, 1103389 and 2018916 to DEG], and the Medical Research Future Fund grants [No 1141334 and 2016199 to DEG].