X-linked Alport syndrome presenting in mother and son with the same unique histopathological features
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
1 Online-Ressource.
- Sprache
-
Englisch
- Erschienen in
-
X-linked Alport syndrome presenting in mother and son with the same unique histopathological features ; volume:37 ; number:3 ; day:26 ; month:4 ; year:2024 ; pages:769-772 ; date:4.2024
Journal of nephrology ; 37, Heft 3 (26.4.2024), 769-772, 4.2024
- Urheber
-
Bergeron, Nicolas A. D.
Garneau, Alexandre P.
Rousseau-Gagnon, Mathieu
Riopel, Julie
Isenring, Paul
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1007/s40620-024-01942-7
- URN
-
urn:nbn:de:101:1-2408112106191.595443563495
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:44 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Bergeron, Nicolas A. D.
- Garneau, Alexandre P.
- Rousseau-Gagnon, Mathieu
- Riopel, Julie
- Isenring, Paul
- SpringerLink (Online service)
Ähnliche Objekte (12)
Sporadic Case of Heterozygous X-Linked Alport Syndrome
Preimplantation Genetic Testing Prevented Intergenerational Transmission of X-Linked Alport Syndrome
A novel COL4A5 splicing variant causing X-linked Alport syndrome: A case report
Novel Digenic Variants in COL4A4 and COL4A5 Causing X-Linked Alport Syndrome: A Case Report
X-linked Alport syndrome: pathogenic variant features and further auditory genotype-phenotype correlations in males
A family case of X-linked Alport syndrome patients with a novel variant in COL4A5
Genotyp-Phänotyp-Korrelation bei Alport-Patientinnen und Alport-Patienten
Pathogenicity of missense variants affecting the collagen IV α5 carboxy non-collagenous domain in X-linked Alport syndrome
Alport, Leo 2
Das Alport-Syndrom
Alport, Leo 3
Alport, Leo 1
Sporadic Case of Heterozygous X-Linked Alport Syndrome
Preimplantation Genetic Testing Prevented Intergenerational Transmission of X-Linked Alport Syndrome
A novel COL4A5 splicing variant causing X-linked Alport syndrome: A case report
Novel Digenic Variants in COL4A4 and COL4A5 Causing X-Linked Alport Syndrome: A Case Report
X-linked Alport syndrome: pathogenic variant features and further auditory genotype-phenotype correlations in males
A family case of X-linked Alport syndrome patients with a novel variant in COL4A5
Genotyp-Phänotyp-Korrelation bei Alport-Patientinnen und Alport-Patienten
Pathogenicity of missense variants affecting the collagen IV α5 carboxy non-collagenous domain in X-linked Alport syndrome
Alport, Leo 2
Das Alport-Syndrom
Alport, Leo 3
Alport, Leo 1
Sporadic Case of Heterozygous X-Linked Alport Syndrome
Preimplantation Genetic Testing Prevented Intergenerational Transmission of X-Linked Alport Syndrome
A novel COL4A5 splicing variant causing X-linked Alport syndrome: A case report
Novel Digenic Variants in COL4A4 and COL4A5 Causing X-Linked Alport Syndrome: A Case Report
X-linked Alport syndrome: pathogenic variant features and further auditory genotype-phenotype correlations in males
A family case of X-linked Alport syndrome patients with a novel variant in COL4A5
Genotyp-Phänotyp-Korrelation bei Alport-Patientinnen und Alport-Patienten
Pathogenicity of missense variants affecting the collagen IV α5 carboxy non-collagenous domain in X-linked Alport syndrome
Alport, Leo 2
Das Alport-Syndrom
Alport, Leo 3