Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity
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author: Daniela A Braun, Edgar A. Otto, John A. Sayer, Heon Yung Gee, Neveen A. Soliman, Jan Halbritter, Rannar Airik, Markus Schueler, Jonathan D Porath, Khemchand Netaram Moorani, Fatih Özaltın, Jennifer Lawson, Shirlee Shril, Bodo B Beck
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