Development of multiple gallstones in a child with lipopolysaccharide-responsive beige-like anchor protein mutation.

KutluÇ§, Seyhan; BoztuÇ§, Kaan; Yildiran, Alisan

KutluÇ§, Seyhan; BoztuÇ§, Kaan; Yildiran, Alisan.

Afiliação

KutluÇ§ S; Department of Paediatric Immunology and Allergy, Faculty of Medicine, Ondokuz Mayis University, Samsun, Turkey.
BoztuÇ§ K; CeMM Research Centre for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Yildiran A; Department of Paediatric Immunology and Allergy, Faculty of Medicine, Ondokuz Mayis University, Samsun, Turkey.

Cent Eur J Immunol ; 44(3): 332-335, 2019.

Article em En | MEDLINE | ID: mdl-31871423

Palavras-chave

Evans syndrome; LRBA deficiency; autoimmune lymphoproliferative syndrome; cholecystectomy; common variable immunodeficiency; gallstones; primary immunodeficiency diseases

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cent Eur J Immunol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Turquia

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