Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis
Titel:
Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis
Auteur:
Daga, Ankana Majmundar, Amar J. Braun, Daniela A. Gee, Heon Yung Lawson, Jennifer A. Shril, Shirlee Jobst-Schwan, Tilman Vivante, Asaf Schapiro, David Tan, Weizhen Warejko, Jillian K. Widmeier, Eugen Nelson, Caleb P. Fathy, Hanan M. Gucev, Zoran Soliman, Neveen A. Hashmi, Seema Halbritter, Jan Halty, Margarita Kari, Jameela A. El-Desoky, Sherif Ferguson, Michael A. Somers, Michael J.G. Traum, Avram Z. Stein, Deborah R. Daouk, Ghaleb H. Rodig, Nancy M. Katz, Avi Hanna, Christian Schwaderer, Andrew L. Sayer, John A. Wassner, Ari J. Mane, Shrikant Lifton, Richard P. Milosevic, Danko Tasic, Velibor Baum, Michelle A. Hildebrandt, Friedhelm