Autosomal dominant tubulointerstitial kidney disease: A review.

Zivná, Martina; Kidd, Kendrah O; Baresová, Veronika; Hulková, Helena; Kmoch, Stanislav; Bleyer, Anthony J

Zivná, Martina; Kidd, Kendrah O; Baresová, Veronika; Hulková, Helena; Kmoch, Stanislav; Bleyer, Anthony J.

Afiliación

Zivná M; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Kidd KO; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Baresová V; Wake Forest University School of Medicine, Section on Nephrology, Winston-Salem, North Carolina, USA.
Hulková H; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Kmoch S; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Bleyer AJ; Research Unit of Rare Diseases, Department of Paediatrics and Inherited Metabolic Disorders, First Faculty of Medicine, Charles University, Prague, Czech Republic.

Am J Med Genet C Semin Med Genet ; 190(3): 309-324, 2022 09.

Article en En | MEDLINE | ID: mdl-36250282

Asunto(s)

Pruebas Genéticas; Insuficiencia Renal Crónica; Humanos; Adulto Joven; Adulto; Persona de Mediana Edad; Anciano; Uromodulina/genética; Mutación

Palabras clave

Autosomal Dominant Tubulointerstitial Kidney Disease; MUC1; REN; UMOD

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Pruebas Genéticas / Insuficiencia Renal Crónica Tipo de estudio: Prognostic_studies Límite: Adult / Aged / Humans / Middle aged Idioma: En Revista: Am J Med Genet C Semin Med Genet Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: República Checa

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