Whole genome sequencing identifies variants associated with sarcoidosis in a family with a high prevalence of sarcoidosis.

Fritz, Daan; Ferwerda, Bart; Brouwer, Matthijs C; van de Beek, Diederik

Fritz, Daan; Ferwerda, Bart; Brouwer, Matthijs C; van de Beek, Diederik.

Afiliação

Fritz D; Department of Neurology, Amsterdam Neuroscience, University of Amsterdam, Amsterdam UMC, P.O. Box 22660, Meibergdreef 9, 1100 DD, Amsterdam, The Netherlands.
Ferwerda B; Department of Neurology, Amsterdam Neuroscience, University of Amsterdam, Amsterdam UMC, P.O. Box 22660, Meibergdreef 9, 1100 DD, Amsterdam, The Netherlands.
Brouwer MC; Department of Neurology, Amsterdam Neuroscience, University of Amsterdam, Amsterdam UMC, P.O. Box 22660, Meibergdreef 9, 1100 DD, Amsterdam, The Netherlands.
van de Beek D; Department of Neurology, Amsterdam Neuroscience, University of Amsterdam, Amsterdam UMC, P.O. Box 22660, Meibergdreef 9, 1100 DD, Amsterdam, The Netherlands. d.vandebeek@amsterdamumc.nl.

Clin Rheumatol ; 40(9): 3735-3743, 2021 Sep.

Article em En | MEDLINE | ID: mdl-33903979

Assuntos

Predisposição Genética para Doença; Sarcoidose; Fatores de Transcrição de Zíper de Leucina Básica/genética; Humanos; Janus Quinase 2/genética; NADPH Oxidases/genética; Prevalência; Sarcoidose/genética; Sequenciamento do Exoma; Sequenciamento Completo do Genoma

Palavras-chave

All genetics; All immunology; Association studies in genetics; Case-control studies

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sarcoidose / Predisposição Genética para Doença Tipo de estudo: Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

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