Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in the SLURP1 gene


  • Present address: R.G.L. Nellen, Department of Dermatology, IJsselland Ziekenhuis, Capelle aan den IJssel, The Netherlands.

  • Funding sources: none.

  • Conflicts of interests: none declared.

Michel van Geel.
E-mail: m.van.geel@mumc.nl

No abstract is available for this article.