Decreased calcium permeability caused by biallelic TRPV5 mutation leads to autosomal recessive renal calcium-wasting hypercalciuria

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Decreased calcium permeability caused by biallelic TRPV5 mutation leads to autosomal recessive renal calcium-wasting hypercalciuria ; volume:32 ; number:11 ; day:25 ; month:3 ; year:2024 ; pages:1506-1514 ; date:11.2024
European journal of human genetics ; 32, Heft 11 (25.3.2024), 1506-1514, 11.2024

Creator: Guleray Lafci, Naz
Goor, Mark van
Cetinkaya, Semra
Wijst, Jenny van der
Acun, Melisa
Kurt Colak, Fatma
Cetinkaya, Arda
Hoenderop, Joost

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41431-024-01589-9

URN: urn:nbn:de:101:1-2502052200161.315164816174

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:32 AM CEST

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Guleray Lafci, Naz
Goor, Mark van
Cetinkaya, Semra
Wijst, Jenny van der
Acun, Melisa
Kurt Colak, Fatma
Cetinkaya, Arda
Hoenderop, Joost
SpringerLink (Online service)

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Decreased calcium permeability caused by biallelic TRPV5 mutation leads to autosomal recessive renal calcium-wasting hypercalciuria

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