Is C1q nephropathy associated with a WDR19 gene mutation? A case report.

Kaynar, K; Güvercin, B; Güler, Ö; Mungan, S; Çaglayan, E

Kaynar, K; Güvercin, B; Güler, Ö; Mungan, S; Çaglayan, E.

Afiliação

Kaynar K; Department of Nephrology, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey.
Güvercin B; Department of Nephrology, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey.
Güler Ö; Department of Internal Medicine, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey.
Mungan S; Department of Pathology, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey.
Çaglayan E; Department of Internal Medicine, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey.

Hippokratia ; 25(2): 87-90, 2021.

Article em En | MEDLINE | ID: mdl-35937515

Palavras-chave

Complement C1q; glomerulonephritis; proteinuria

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2021 Tipo de documento: Article