A Novel Homozygous KLHL3 Mutation as a Cause of Autosomal Recessive Pseudohypoaldosteronism Type II Diagnosed Late in Life
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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Online-Ressource
- Sprache
-
Englisch
- Erschienen in
-
In: 10.1159/000521626
- Ereignis
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Veröffentlichung
- (wo)
-
Aachen
- (wer)
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Universitätsbibliothek der RWTH Aachen
- (wann)
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2022
- Urheber
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Etges, Annika
Hellmig, Nicole
Walenda, Gudrun
Haddad, Bassam G.
Machtens, Jan-Philipp
Morosan, Thomas
Rump, Lars Christian
Scholl, Ute I.
- DOI
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10.18154/RWTH-CONV-251131
- URN
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urn:nbn:de:101:1-2023051801355030067481
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
25.03.2025, 13:43 MEZ
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Beteiligte
- Etges, Annika
- Hellmig, Nicole
- Walenda, Gudrun
- Haddad, Bassam G.
- Machtens, Jan-Philipp
- Morosan, Thomas
- Rump, Lars Christian
- Scholl, Ute I.
- Universitätsbibliothek der RWTH Aachen
Entstanden
- 2022
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