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, Jeremiah; Liu, Qingxue; Vukojevic, Katarina; Ke, Juntao; Lim, Tze Y.; Khan, Atlas; Gupta, Yask; Perez, Alejandra; Yan, Zonghai; Milo Rasouly, Hila; Vena, Natalie; Lippa, Natalie; Giordano, Jessica L.; Saraga, Marijan; Saraga-Babic, Mirna; Westland, Rik; Bodria, Monica; Piaggio, Giorgio; Bendapudi, Pavan K.; Iglesias, Alejandro D.; Wapner, Ronald J.; Tasic, Velibor; Wang, Fan; Ionita-Laza, Iuliana; Ghiggeri, Gian Marco; Kiryluk, Krzysztof; Sampogna, Rosemary V.; Mendelsohn, Cathy L.; D’Agati, Vivette D.; Gharavi, Ali G.; Sanna-Cherchi, Simone
Source
In Genetics in Medicine December 2023 25(12)
Subject
Language
ISSN
1098-3600