Conflict of interest: the authors declare that they have no conflicts of interest.
Experimental dermatology ● Original article
New intragenic and promoter region deletion mutations in FERMT1 underscore genetic homogeneity in Kindler syndrome
Article first published online: 18 MAR 2014
© 2014 British Association of Dermatologists
Clinical and Experimental Dermatology
Volume 39, Issue 3, pages 361–367, April 2014
How to Cite
Fuchs-Telem, D., Nousbeck, J., Singer, A., McGrath, J. A., Sarig, O. and Sprecher, E. (2014), New intragenic and promoter region deletion mutations in FERMT1 underscore genetic homogeneity in Kindler syndrome. Clinical and Experimental Dermatology, 39: 361–367. doi: 10.1111/ced.12222
The first two authors contributed equally to this work and should be considered joint first authors.
- Issue published online: 18 MAR 2014
- Article first published online: 18 MAR 2014
- Manuscript Accepted: 9 MAY 2013
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