Skip to content
VuFind
    • English
    • Deutsch
    • Español
    • Français
    • Italiano
    • 日本語
    • Nederlands
    • Português
    • Português (Brasil)
    • 中文(简体)
    • 中文(繁體)
    • Türkçe
    • עברית
    • Gaeilge
    • Cymraeg
    • Ελληνικά
    • Català
    • Euskara
    • Русский
    • Čeština
    • Suomi
    • Svenska
    • polski
    • Dansk
    • slovenščina
    • اللغة العربية
    • বাংলা
    • Galego
    • Tiếng Việt
    • Hrvatski
    • हिंदी
    • Հայերէն
    • Українська
    • Sámegiella
    • Монгол
Advanced
  • ANKYLOSING SPONDYLITIS IS STRO...
  • Cite this
  • Text this
  • Email this
  • Print
  • Export Record
    • Export to RefWorks
    • Export to EndNoteWeb
    • Export to EndNote
  • Permanent link
ANKYLOSING SPONDYLITIS IS STRONGLY ASSOCIATED WITH VARIANTS IN THE CMG2 GENE

ANKYLOSING SPONDYLITIS IS STRONGLY ASSOCIATED WITH VARIANTS IN THE CMG2 GENE

Bibliographic Details
Main Authors: Karaderi, T, Cohen, C, Keidel, S, Appleton, L, Macfarlane, G, Siebert, S, Evans, D, Wordsworth, B
Format: Conference item
Published: 2013
  • Holdings
  • Description
  • Similar Items
  • Staff View

Similar Items

  • ANTXR2 IS ASSOCIATED WITH ANKYLOSING SPONDYLITIS
    by: Karaderi, T, et al.
    Published: (2014)
  • Ankylosing spondylitis is associated with the anthrax toxin receptor 2 gene (ANTXR2).
    by: Karaderi, T, et al.
    Published: (2014)
  • Ankylosing spondylitis is associated with the anthrax toxin receptor 2 gene (ANTXR2)
    by: Karaderi, T, et al.
    Published: (2014)
  • A CCR6 variant strongly associated with rheumatoid arthritis in two populations is not associated with ankylosing spondylitis
    by: Cohen, CJ, et al.
    Published: (2012)
  • EPIGENETIC REGULATION OF THE IL-23R LOCUS IN ANKYLOSING SPONDYLITIS
    by: Cohen, C, et al.
    Published: (2013)

Search Options

  • Search History
  • Advanced Search

Find More

  • Browse the Catalog
  • Browse Alphabetically
  • Explore Channels
  • Course Reserves
  • New Items

Need Help?

  • Search Tips
  • Ask a Librarian
  • FAQs