Title |
Precise variant interpretation, phenotype ascertainment, and genotype–phenotype correlation of children in the EARLY PRO‐TECT Alport trial / Jan Boeckhaus, Julia Hoefele, Korbinian M. Riedhammer, Burkhard Tönshoff, Rasmus Ehren, Lars Pape, Kay Latta, Henry Fehrenbach, Baerbel Lange‐Sperandio, Matthias Kettwig, Peter Hoyer, Hagen Staude, Martin Konrad, Ulrike John, Jutta Gellermann, Bernd Hoppe, Matthias Galiano, Michaela Gessner, Michael Pohl, Carsten Bergmann, Tim Friede, Oliver Gross |
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Involved |
Jan Simon Böckhaus (Verfasser)
Julia Höfele (Verfasser) Korbinian M. Riedhammer (Verfasser) Burkhard Tönshoff (Verfasser)
Rasmus Ehren (Verfasser)
Lars Pape (Verfasser) Kay Latta (Verfasser) Henry Fehrenbach (Verfasser) Baerbel Lange‐Sperandio (Verfasser) Matthias Kettwig (Verfasser) Peter Hoyer (Verfasser) Hagen Staude (Verfasser) Martin Konrad (Verfasser) Ulrike John-Kroegel (Verfasser) Jutta Gellermann (Verfasser) Bernd Hoppe (Verfasser) Matthias Galiano (Verfasser) Michaela Gessner (Verfasser) Michael Pohl (Verfasser) Carsten Bergmann (Verfasser) Tim Friede (Verfasser) Oliver Gross (Verfasser) |
Published |
Erlangen: Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU) |
Extent |
Online-Ressource |
Language |
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Country |
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Topic |
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Subject |
Alport syndrome |
DDC notation |
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Persistent identifier |
urn:nbn:de:bvb:29-opus4-159653 (URN) |
Further information |
In: Clinical Genetics 99.1 (2021): S. 143-156. <https://onlinelibrary.wiley.com/doi/10.1111/cge.13861> |
Record ID |
1228627738 |
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