The functional R620W variant of the PTPN22 gene is associated with celiac disease.

No abstract is available for this paper.

• Publication year

  2008

• Venue

  Tissue Antigens

• Publication date

  2008-03-01

• Fields of study

  Medicine

• Identifiers
  DOI 10.1111/j.1399-0039.2007.01002.xPMID 18194365
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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  2005cited by this paper
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  2004cited by this paper
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  2004cited by this paper
• Coeliac disease.

  2003cited by this paper
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  2002cited by this paper
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  2002cited by this paper
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  2001cited by this paper
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  1998cited by this paper
• Fits and Faints

  1991cited by this paper
• Revised criteria for diagnosis of coeliac disease. Report of Working Group of European Society of Paediatric Gastroenterology and Nutrition.

  1990influential reference

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  2023cites this paper
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  2019cites this paper
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  2017influential citation
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  2017influential citation
• STUDIES OF MUCOSAL IMMUNE REGULATION IN CELIAC DISEASE AND TYPE 1 DIABETES

  2014cites this paper
• Coherent Somatic Mutation in Autoimmune Disease

  2014cites this paper
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  2014cites this paper
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  2014cites this paper
• Chapter 86 – Diabetes Mellitus

  2013cites this paper
• Desarrollos metodológicos para el análisis de polimorfismos de los genes del sistema HLA y otros genes, no HLA, predisponentes a enfermedades autoinmunes

  2013cites this paper
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  2012cites this paper
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  2011cites this paper
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  2011cites this paper
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  2010cites this paper
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  2010cites this paper
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  2010cites this paper
• Genetic Variation and Expression of the IRF5 Gene in Autoimmune Diseases

  2009cites this paper
• Recent advances in coeliac disease

  2009cites this paper
• Insights into the molecular genetics of celiac disease : Applying family- and population-based strategies

  2009cites this paper
• INSIGHTS INTO THE MOLECULAR GENETICS OF CELIAC DISEASE

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  2008cites this paper
• GB virus type C-driven protection in HIV/HCV coinfection: possible role of interferon gamma and dendritic cell activation.

  2008cites this paper