Associated Papers
Disease-causing mutations in the G protein β5 β-propeller disrupt its chaperonin-mediated folding trajectory.
Sass MI et al.
Biorxiv : the Preprint Server for Biology, 2025
Inhibition of G-protein signalling in cardiac dysfunction of intellectual developmental disorder with cardiac arrhythmia (IDDCA) syndrome.
De Nittis P et al.
Journal of Medical Genetics, 2021
Intellectual developmental disorder with cardiac arrhythmia syndrome in a child with compound heterozygous GNB5 variants.
Vernon H et al.
Clinical Genetics, 2018
A NGS-Targeted Autism/ID Panel Reveals Compound Heterozygous GNB5 Variants in a Novel Patient.
Malerba N et al.
Frontiers in Genetics, 2018
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