Unusual cutaneous features associated with a heterozygous gain-of-function mutation inIFIH1: overlap between Aicardi-Goutières and Singleton-Merten syndromes

  • A.-C. Bursztejn, T.A. Briggs, Y. del Toro Duany, B.H. Anderson, J. O'Sullivan, S.G. Williams, C. Bodemer, S. Fraitag, F. Gebhard, B. Leheup, I. Lemelle, A. Oojageer, E. Raffo, E. Schmitt, G.I. Rice, S. Hur, Y.J. Crow
  • British Journal of Dermatology, October 2015, Wiley
  • DOI: 10.1111/bjd.14073

The authors haven't yet claimed this publication.

Read Publication


In partnership with:

Link to Wiley showcase