- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2369
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Non-collagen genes role in digenic Alport syndrome ; volume:20 ; number:1 ; day:26 ; month:2 ; year:2019 ; pages:1-9 ; date:12.2019
BMC nephrology ; 20, Heft 1 (26.2.2019), 1-9, 12.2019
- Creator
-
Daga, S.
Fallerini, C.
Furini, S.
Pecoraro, C.
Scolari, F.
Ariani, F.
Bruttini, M.
Mencarelli, M. A.
Mari, F.
Renieri, A.
Pinto, A. M.
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s12882-019-1258-5
- URN
-
urn:nbn:de:101:1-2019032423443235337183
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:48 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Daga, S.
- Fallerini, C.
- Furini, S.
- Pecoraro, C.
- Scolari, F.
- Ariani, F.
- Bruttini, M.
- Mencarelli, M. A.
- Mari, F.
- Renieri, A.
- Pinto, A. M.
- SpringerLink (Online service)
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Pathogenicity of missense variants affecting the collagen IV α5 carboxy non-collagenous domain in X-linked Alport syndrome
Molecular pathology and genetics of alport syndrome : 19 tables
Explaining Alport syndrome—lessons from the adult nephrology clinic
Finerenone and other future therapeutic options for Alport syndrome
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iPSC-derived type IV collagen α5-expressing kidney organoids model Alport syndrome
Molecular testing for adult type Alport syndrome
SGLT2-inhibition in patients with Alport syndrome
Severe restless legs syndrome in a family with Alport syndrome
Sporadic Case of Heterozygous X-Linked Alport Syndrome
Pathogenicity of missense variants affecting the collagen IV α5 carboxy non-collagenous domain in X-linked Alport syndrome
Molecular pathology and genetics of alport syndrome : 19 tables
Explaining Alport syndrome—lessons from the adult nephrology clinic
Finerenone and other future therapeutic options for Alport syndrome
Correction to: Severe restless legs syndrome in a family with Alport syndrome
Genotyp-Phänotyp-Korrelation bei Alport-Patientinnen und Alport-Patienten
Four novel mutations identified in the COL4A3, COL4A4 and COL4A5 genes in 10 families with Alport syndrome
iPSC-derived type IV collagen α5-expressing kidney organoids model Alport syndrome
Molecular testing for adult type Alport syndrome
SGLT2-inhibition in patients with Alport syndrome
Severe restless legs syndrome in a family with Alport syndrome
Sporadic Case of Heterozygous X-Linked Alport Syndrome
Pathogenicity of missense variants affecting the collagen IV α5 carboxy non-collagenous domain in X-linked Alport syndrome
Molecular pathology and genetics of alport syndrome : 19 tables
Explaining Alport syndrome—lessons from the adult nephrology clinic
Finerenone and other future therapeutic options for Alport syndrome
Correction to: Severe restless legs syndrome in a family with Alport syndrome
Genotyp-Phänotyp-Korrelation bei Alport-Patientinnen und Alport-Patienten