Year: 2025
Type: article
Abstract: The aim of this Congress was to bring together clinicians and researchers working in the area of Fragile X Syndrome (FXS) and Fragile X Premutation Associated Conditions (FXPAC) from around the world, giving them the opportunity to network, be informed of the latest research from colleagues, workshop ideas through panel discussions, discuss translational research with clinical applications, and form relationships of future collaboration.The speakers' presentations covered various FMR1 premutation issues, biomarkers, behavioural aspects, treatment of FXS, mosaicism, models of care and expert centres in various countries, and more.A recently published paper, 'A Holis tic Appro ach to Fragi le X Syndr ome' , was presented and provides the reader with an overview of the scope of the Congress.Prof Scerif's contribution was supported by ESRC UKRI grant ES/X013561/1.
Authors: 2025, : P1
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,990
Funders: Children’s Hospital of Wisconsin Research Institute, UK Research and Innovation, Murdoch Children's Research Institute, Australian Government, European Commission, University of Technology Sydney, Monash University, University of Adelaide, Economic and Social Research Council, Instituto de Salud Carlos III
OpenAlex ID: W4409771803