CARD15 mutations in Blau syndrome

  • Miceli-Richard C
  • Lesage S
  • Rybojad M
 et al. 
  • 96

    Readers

    Mendeley users who have this article in their library.
  • 648

    Citations

    Citations of this article.

Abstract

We have identified three missense mutations in the nucleotide-binding domain (NBD) of CARD15/NOD2 in four French and German families with Blau syndrome. Our findings indicate that, in addition to Crohn disease, CARD15 is involved in the susceptibility to a second granulomatous disorder.

Get free article suggestions today

Mendeley saves you time finding and organizing research

Sign up here
Already have an account ?Sign in

Find this document

Authors

Cite this document

Choose a citation style from the tabs below

Save time finding and organizing research with Mendeley

Sign up for free