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Molecular consequences of PQBP1 deficiency, involved in the X-linked Renpenning syndrome
Document Type
Article
Author
Courraud, J.; Engel, C.; Quartier, A.; Drouot, N.; Houessou, U.; Plassard, D.; Mandel, J.-L.; Piton, A.; Sorlin, A.; Brischoux-Boucher, E.; Van Maldergem, L.; Gouy, E.; Rossi, M.; Lesca, G.; Edery, P.; Putoux, A.; Bilan, F.; Gilbert-Dussardier, B.; Atallah, I.; Kalscheuer, V.M.
Source
In: Molecular Psychiatry. (Molecular Psychiatry, February 2024, 29(2):287-296)
Subject
Language
English
ISSN
14765578
13594184

Online Access

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