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Project
Unraveling the role of the KEOPS complex in Galloway-Mowat syndrome
Information
Project Team
Organisations
Outputs & Impact
Publications & research data ( 2 )
Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder
Maria del Rocio Pérez Baca
María Palomares-Bralo
Michiel Vanhooydonck
Lisa Hamerlinck
Eva D'haene
Sebastian Leimbacher
Eva Jacobs
Laurenz De Cock
Erika D'haenens
Annelies Dheedene
et al.
A1
Journal Article
in
AMERICAN JOURNAL OF HUMAN GENETICS
2025
Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability
Maria del Rocio Pérez Baca
Eva Jacobs
Lies Vantomme
Pontus LeBlanc
Elke Bogaert
Annelies Dheedene
Laurenz De Cock
Sadegheh Haghshenas
Aidin Foroutan
Michael A Levy
et al.
A1
Journal Article
in
AMERICAN JOURNAL OF HUMAN GENETICS
2024
Activities ( 0 )
Results
Impact narratives ( 0 )
Patents ( 0 )