Diverse retinal-kidney phenotypes associated with NPHP1 homozygous whole-gene deletions in patients with kidney failure
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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1 Online-Ressource.
- Sprache
-
Englisch
- Erschienen in
-
Diverse retinal-kidney phenotypes associated with NPHP1 homozygous whole-gene deletions in patients with kidney failure ; volume:3 ; number:1 ; day:1 ; month:3 ; year:2024 ; pages:1-8 ; date:12.2024
Journal of rare diseases ; 3, Heft 1 (1.3.2024), 1-8, 12.2024
- Klassifikation
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Medizin, Gesundheit
- Urheber
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Esson, Gavin
Logan, Ian
Wood, Katrina
Browning, Andrew C.
Sayer, John A.
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1007/s44162-024-00031-4
- URN
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urn:nbn:de:101:1-2404180708092.175409164063
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:50 MESZ
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Beteiligte
- Esson, Gavin
- Logan, Ian
- Wood, Katrina
- Browning, Andrew C.
- Sayer, John A.
- SpringerLink (Online service)
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