Article info

Download PDFPDF
Original article
Mutation in KANK2, encoding a sequestering protein for steroid receptor coactivators, causes keratoderma and woolly hair

Authors

  1. Correspondence to Professor Abraham Zlotogorski, Department of Dermatology, Hadassah—Hebrew University Medical Center, Jerusalem 9112001, Israel; zloto{at}cc.huji.ac.il
View Full Text

Citation

Ramot Y, Molho-Pessach V, Meir T, et al
Mutation in KANK2, encoding a sequestering protein for steroid receptor coactivators, causes keratoderma and woolly hair

Publication history

  • Received February 19, 2014
  • Revised February 27, 2014
  • Accepted February 28, 2014
  • First published March 26, 2014.
Online issue publication 
May 17, 2014

Article Versions

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.