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Dive into the research topics of 'Five novel mutations in the SCNN1A gene causing autosomal recessive pseudohypoaldosteronism type 1'. Together they form a unique fingerprint.- Sort by
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Maik Welzel, Leyla Akin, Anja Büscher, Tülay Güran, Berthold P Hauffa, Wolfgang Högler, Julia Leonards, Beate Karges, Heiner Kentrup, Birgul Kirel, Emine Esin Yalinbas Senses, Neslihan Tekin, Paul-Martin Holterhus, Felix G Riepe
Research output: Contribution to journal › Article › peer-review