Hemizygous variants in protein phosphatase 1 regulatory subunit 3F (PPP1R3F) are associated with a neurodevelopmental disorder characterized by developmental delay, intellectual disability and autistic features
ZG Liu, BZ Xin, IN Smith, V Sency, J Szekely, A Alkelai, A Shuldiner, S Efthymiou, F Rajabi, S Coury, CA Brownstein, S Rudnik-Schoeneborn, AL Bruel, J Thevenon, S Zeidler, P Jayakar, A Schmidt, K Cremer, H Engels, SO PetersMS Zaki, RZ Duan, CL Zhu, YR Xu, C Gao, T Sepulveda-Morales, R Maroofian, IA Alkhawaja, M Khawaja, H Alhalasah, H Houlden, JA Madden, V Turchetti, D Marafi, PB Agrawal, U Schatz, A Rotenberg, J Rotenberg, GMS Mancini, S Bakhtiari, M Kruer, I Thiffault, S Hirsch, M Hempel, LG Stuehn, TB Haack, JE Posey, JR Lupski, HYP Lee, NB Sarn, C Eng, C Gonzaga-Jauregui*, B Zhang, H Wang*
Research output: Contribution to journal › Article › Academic › peer-review
2Citations
(Scopus)
Fingerprint
Dive into the research topics of 'Hemizygous variants in protein phosphatase 1 regulatory subunit 3F (PPP1R3F) are associated with a neurodevelopmental disorder characterized by developmental delay, intellectual disability and autistic features'. Together they form a unique fingerprint.