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

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http://dx.doi.org/10.1111/bjd.14073

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