A Rare STXBP2 Mutation in Severe COVID-19 and Secondary Cytokine Storm Syndrome.

Reiff, Daniel D; Zhang, Mingce; Smitherman, Emily A; Mannion, Melissa L; Stoll, Matthew L; Weiser, Peter; Cron, Randy Q

Reiff, Daniel D; Zhang, Mingce; Smitherman, Emily A; Mannion, Melissa L; Stoll, Matthew L; Weiser, Peter; Cron, Randy Q.

Afiliación

Reiff DD; Department of Pediatrics, Division of Rheumatology, University of Alabama at Birmingham, Birmingham, AL 35233-1711, USA.
Zhang M; Department of Pediatrics, Division of Rheumatology, University of Alabama at Birmingham, Birmingham, AL 35233-1711, USA.
Smitherman EA; Department of Pediatrics, Division of Rheumatology, University of Alabama at Birmingham, Birmingham, AL 35233-1711, USA.
Mannion ML; Department of Pediatrics, Division of Rheumatology, University of Alabama at Birmingham, Birmingham, AL 35233-1711, USA.
Stoll ML; Department of Pediatrics, Division of Rheumatology, University of Alabama at Birmingham, Birmingham, AL 35233-1711, USA.
Weiser P; Department of Pediatrics, Division of Rheumatology, University of Alabama at Birmingham, Birmingham, AL 35233-1711, USA.
Cron RQ; Department of Pediatrics, Division of Rheumatology, University of Alabama at Birmingham, Birmingham, AL 35233-1711, USA.

Life (Basel) ; 12(2)2022 Jan 20.

Article en En | MEDLINE | ID: mdl-35207437

Palabras clave

COVID-19; cytokine storm syndrome; cytolysis; degranulation; genetics; hemophagocytic lymphohistiocytosis; macrophage activation syndrome; mutation; natural killer cell

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Life (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza

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