학술논문
Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder
Document Type
Article
Author
Dias, C.M.; Partlow, J.N.; Walsh, C.A.; Punetha, J.; Pehlivan, D.; Posey, J.E.; Mitani, T.; Coban-Akdemir, Z.; Karaca, E.; Lupski, J.R.; Zheng, C.; Orlova, V.; Seiradake, E.; Mazaheri, N.; Galehdari, H.; Shariati, G.; Rad, A.; Efthymiou, S.; Salpietro, V.; Houlden, H.; Maroofian, R.; Petersen, A.; Durham, L.; Dehghani, M.; Vahidi Mehrjardi, M.Y.; Gezdirici, A.; Malamiri, R.A.; Al Menabawy, N.M.; Selim, L.A.; Banu, S.; Polla, D.L.; van Beusekom, E.; Schaeken, L.L.M.; van Bokhoven, H.; Yang, E.; Rezazadeh Varaghchi, J.; Najafi, M.; Sedaghat, A.; Keller-Ramey, J.; Sherafat, A.; Jhangiani, S.N.; Stanley, V.; Gleeson, J.G.
Source
In: American Journal of Human Genetics . (American Journal of Human Genetics, 7 November 2019, 105(5):1048-1056)
Subject
Language
English
ISSN
15376605
00029297
00029297