Conflict of interests: none.
LETTERS TO THE EDITOR
Case of Kindler syndrome resulting from mutation in the FERMT1 gene
Article first published online: 6 JUN 2012
© 2012 Japanese Dermatological Association
The Journal of Dermatology
Volume 39, Issue 12, pages 1057–1058, December 2012
How to Cite
WADA, M., MASUDA, K., TSURUTA, D., TAMAI, K., LAI-CHEONG, J. E., McGRATH, J. A. and KATOH, N. (2012), Case of Kindler syndrome resulting from mutation in the FERMT1 gene. The Journal of Dermatology, 39: 1057–1058. doi: 10.1111/j.1346-8138.2012.01598.x
Funding sources: none.
- Issue published online: 26 NOV 2012
- Article first published online: 6 JUN 2012