Entry details

Courtois et al. (2003) "A hypermorphic IkappaBalpha mutation is associated with autosomal dominant anhidrotic ectodermal dysplasia and T cell immunodeficiency." J. Clin. Invest. 112(7):1108-1115 (PubMed)

Cited by (in linked databases)

  1. NFKBIA, nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, alpha GenAge: Human Ageing-Associated Genes