ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling
Heon Yung Gee(Yonsei University), Friedhelm Hildebrandt(Boston Children's Hospital), Neveen A. Soliman(Cairo University), Lutz T. Weber(University Hospital Cologne), Jeffrey W. Innis(University of Michigan), Weibin Zhou(University of Michigan), Roger C. Wiggins(University of Michigan), Toby W. Hurd(University of Michigan–Ann Arbor), Dominik S. Schoeb(University of Michigan), Gil Chernin(Hebrew University of Jerusalem), Shawn Levy(HudsonAlpha Institute for Biotechnology), Virginia Vega-Warner(University of Michigan), Shazia Ashraf(Riphah International University), Julia Hoefele(Institute of Human Genetics), Joseph Washburn, Hanan Fathy(Alexandria University), Olivier Gribouval(Inserm), Pawaree Saisawat(University of Michigan), Edgar A. Otto(University of Michigan), Corinne Antignac(Hôpital Necker-Enfants Malades), Yaacov Frishberg(Shaare Zedek Medical Center), Christian Faul(University of Miami), Bodo B. Beck(University of Cologne), Zhe Han(University of Maryland, Baltimore), Buğsu Övünç(Dartmouth College), Heike Goebel(Taipei Institute of Pathology), Humphrey Fang(Boston Children's Hospital), S. Natarajan(University of Michigan), Katrina A. Diaz(University of Michigan), Svjetlana Lovric(Boston Children's Hospital)
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