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Original article
Mutation in KANK2, encoding a sequestering protein for steroid receptor coactivators, causes keratoderma and woolly hair
- Correspondence to Professor Abraham Zlotogorski, Department of Dermatology, Hadassah—Hebrew University Medical Center, Jerusalem 9112001, Israel; zloto{at}cc.huji.ac.il
Citation
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
April 27, 2016
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- Previous version (27 April 2016).
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