학술논문
Heterozygous variants in PRPF8 are associated with neurodevelopmental disorders
Document Type
Article
Author
O'Grady, L.; Sweetser, D.A.; Gold, N.B.; Schrier Vergano, S.A.; Hoffman, T.L.; Sarco, D.; Cherny, S.; Bryant, E.; Schultz-Rogers, L.; Chung, W.K.; Sacharow, S.; Rodan, L.; Immken, L.L.; Holder, S.; Blackwell, R.R.; Buchanan, C.; Yusupov, R.; Lecoquierre, F.; Guerrot, A.-M.; de Vries, B.B.A.; Kamsteeg, E.J.; Santos Simarro, F.; Palomares-Bralo, M.; Brown, N.; Pais, L.; Ferrer, A.; Klee, E.W.; Babovic-Vuksanovic, D.; Rhodes, L.; Person, R.; Begtrup, A.; Keller-Ramey, J.; Santiago-Sim, T.; Schnur, R.E.
Source
In: American Journal of Medical Genetics, Part A . (American Journal of Medical Genetics, Part A, September 2022, 188(9):2750-2759)
Subject
Language
English
ISSN
15524833
15524825
15524825