Kalscheuer, Vera M. Chromosome Rearrangements and Disease (Vera Kalscheuer), Research Group Development & Disease (Head: Stefan Mundlos), Max Planck Institute for Molecular Genetics, Max Planck Society;
MolPsychiatry_Courraud et al_2023.pdf (Verlagsversion), 3MB
Courraud, J., Engel, C., Quartier, A., Drouot, N., Houessou, U., Plassard, D., et al. (2023). Molecular consequences of PQBP1 deficiency, involved in the X-linked Renpenning syndrome. Molecular Psychiatry. doi:10.1038/s41380-023-02323-5.