Whole exome sequencing identifies causative mutations in...

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Kidney International 2015 / 10

Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity

Braun, Daniela A, Schueler, Markus, Halbritter, Jan, Gee, Heon Yung, Porath, Jonathan D, Lawson, Jennifer A, Airik, Rannar, Shril, Shirlee, Allen, Susan J, Stein, Deborah, Al Kindy, Adila, Beck, Bodo
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Language:
english
Journal:
Kidney International
DOI:
10.1038/ki.2015.317
Date:
October, 2015
File:
PDF, 206 KB
english, 2015
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