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Dive into the research topics of 'Detection of DZIP1L mutations by whole-exome sequencing in consanguineous families with polycystic kidney disease'. Together they form a unique fingerprint.- Sort by
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Jens Michael Hertz, Per Svenningsen, Henrik Dimke, Morten Buch Engelund, Hanne Nørgaard, Anita Hansen, Niels Marcussen, Helle Charlotte Thiesson, Carsten Bergmann, Martin J Larsen