Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity
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| Description | scientific article |
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author: Fatih Ozaltin Edgar A. Otto Neveen A. Soliman Jennifer Lawson Rannar Airik John A. Sayer Jonathan D Porath Markus Schueler Shirlee Shril Heon Yung Gee Jan Halbritter Khemchand Netaram Moorani Bodo B Beck Daniela A Braun |
| Publication date | October 21, 2015 |
| Language | English |
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