Author Renders, Lutz

1 to 2 of 2 Items
  • 2019 | Journal Article | 
    ​ ​The Hypomorphic Variant p.(Gly624Asp) in COL4A5 as a Possible Cause for an Unexpected Severe Phenotype in a Family With X-Linked Alport Syndrome​
    Macheroux, E. P.; Braunisch, M. C.; Pucci Pegler, S.; Satanovskij, R.; Riedhammer, K. M.; Günthner, R. & Gross, O.  et al.​ (2019) 
    Frontiers in Pediatrics, 7.​ DOI: https://doi.org/10.3389/fped.2019.00485 
    ​Details  DOI 
  • 2022 | Journal Article | 
    ​ ​The multifaceted phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy—A human genetics department experience​
    Ćomić, J.; Riedhammer, K. M.; Günthner, R.; Schaaf, C. W.; Richthammer, P.; Simmendinger, H. & Kieffer, D. et al.​ (2022) 
    Frontiers in Medicine, 9 art. 957733​.​ DOI: https://doi.org/10.3389/fmed.2022.957733 
    ​Details  DOI 

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Göttingen All

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