Conflicts of interest None to declare.
Prevalent founder mutation c.736T>A of LIPH in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood
Article first published online: 26 MAR 2012
© 2012 The Authors. Journal of the European Academy of Dermatology and Venereology © 2012 European Academy of Dermatology and Venereology
Journal of the European Academy of Dermatology and Venereology
Volume 27, Issue 9, pages 1182–1184, September 2013
How to Cite
Tanahashi, K., Sugiura, K., Takeichi, T., Takama, H., Shinkuma, S., Shimizu, H. and Akiyama, M. (2013), Prevalent founder mutation c.736T>A of LIPH in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood. Journal of the European Academy of Dermatology and Venereology, 27: 1182–1184. doi: 10.1111/j.1468-3083.2012.04526.x
Funding sources This study was supported in part by a Grant-in-Aid for Scientific Research, (A) 23249058 (M.A.) from the Ministry of Education, Culture, Sports, Science and Technology of Japan.
- Issue published online: 28 JUL 2013
- Article first published online: 26 MAR 2012
- Received: 1 February 2012; Accepted: 27 February 2012
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