Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity
Daniela A. Braun(University Hospital Münster), Friedhelm Hildebrandt(Boston Children's Hospital), Neveen A. Soliman(Cairo University), Detlef Böckenhauer(Great Ormond Street Hospital for Children NHS Foundation Trust), Fatih Özaltın(University of Michigan), Rannar Airik(University of Michigan), Khemchand N Moorani(National Institute of Child Health), John A. Sayer(Newcastle University), Richard P. Lifton(Rockefeller University), Nurcan Cengız(Başkent University), Heon Yung Gee(Yonsei University), Edgar A. Otto(University of Michigan), Shirlee Shril(MACOM (United States)), Adila Al Kindy(Sultan Qaboos University), Jonathan D. Porath, Deborah R. Stein, Bodo B. Beck(University of Cologne), Markus Schueler(Boston Children's Hospital), Jennifer A. Lawson, Susan J. Allen(University of Michigan), Seema Hashmi, Jan Halbritter(Charité - Universitätsmedizin Berlin)
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