Factor B Mutation in Monozygotic Twins Discordant for Atypical Hemolytic Uremic Syndrome.

Aradottir, Sigridur Sunna; Kristoffersson, Ann-Charlotte; Jensson, Brynjar O; Sulem, Patrick; Gong, Henning; Palsson, Runolfur; Karpman, Diana

Aradottir, Sigridur Sunna; Kristoffersson, Ann-Charlotte; Jensson, Brynjar O; Sulem, Patrick; Gong, Henning; Palsson, Runolfur; Karpman, Diana.

Afiliación

Aradottir SS; Department of Pediatrics, Clinical Sciences Lund, Lund University, Lund, Sweden.
Kristoffersson AC; Department of Pediatrics, Clinical Sciences Lund, Lund University, Lund, Sweden.
Jensson BO; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
Sulem P; deCODE genetics/Amgen Inc., Reykjavik, Iceland.
Gong H; Department of Pediatrics, Clinical Sciences Lund, Lund University, Lund, Sweden.
Palsson R; Landspitali-The National University Hospital of Iceland, Reykjavik, Iceland.
Karpman D; University of Iceland, Reykjavik, Iceland.

Kidney Int Rep ; 8(5): 1097-1101, 2023 May.

Article en En | MEDLINE | ID: mdl-37180503

Palabras clave

Factor B; atypical hemolytic uremic syndrome; complement; genetics; monozygotic twins

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Kidney Int Rep Año: 2023 Tipo del documento: Article País de afiliación: Suecia

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