학술논문
Null and missense mutations of ERI1 cause a recessive phenotypic dichotomy in humans
Document Type
Article
Author
Guo, L.; Xue, J.-Y.; Salian, S.; Rousseau, J.; Kim, H.; Campeau, P.M.; Wang, Z.; Wei, Z.-J.; Nishimura, G.; Ikegawa, S.; Rath, N.; Heissmeyer, V.; Ehresmann, S.; Moosa, S.; Nakagawa, N.; Kuroda, H.; Clayton-Smith, J.; Banka, S.; Jackson, A.; Wang, J.; Zhang, Y.-M.; Hüning, I.; Brunet, T.; Ohashi, H.; Thomas, M.F.; Bupp, C.; Miyake, N.; Matsumoto, N.; Mendoza-Londono, R.; Costain, G.; Di Donato, N.; Yamada, T.; Ansel, K.M.; Yigit, G.; Wollnik, B.; Hrabě de Angelis, M.; Mégarbané, A.; Hahn, G.; Rosenfeld, J.A.
Source
In: American Journal of Human Genetics . (American Journal of Human Genetics, 6 July 2023, 110(7):1068-1085)
Subject
Language
English
ISSN
15376605
00029297
00029297