학술논문
Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies
Document Type
Article
Author
Martino, J.; Liu, Q.; Vukojevic, K.; Ke, J.; Lim, T.Y.; Khan, A.; Gupta, Y.; Perez, A.; Yan, Z.; Milo Rasouly, H.; Vena, N.; Lippa, N.; Kiryluk, K.; Sampogna, R.V.; Gharavi, A.G.; Sanna-Cherchi, S.; Saraga-Babic, M.; Giordano, J.L.; Wapner, R.J.; Saraga, M.; Westland, R.; Bodria, M.; Piaggio, G.; Ghiggeri, G.M.; Bendapudi, P.K.; Iglesias, A.D.; Tasic, V.; Wang, F.; Ionita-Laza, I.; Mendelsohn, C.L.; D'Agati, V.D.
Source
In: Genetics in Medicine . (Genetics in Medicine, December 2023, 25(12))
Subject
Language
English
ISSN
15300366
10983600
10983600