Funding sources: none.
Letters to the Editor
Erythrokeratodermia variabilis: First Japanese case documenting GJB3 mutation
Article first published online: 27 FEB 2013
© 2013 Japanese Dermatological Association
The Journal of Dermatology
Special Issue: Special Issue: Genetics of hypopigmentary disorders (pages 309-356)
Volume 40, Issue 5, pages 402–403, May 2013
How to Cite
Ikeya, S., Urano, S., Sakabe, J.-i., Ito, T. and Tokura, Y. (2013), Erythrokeratodermia variabilis: First Japanese case documenting GJB3 mutation. The Journal of Dermatology, 40: 402–403. doi: 10.1111/1346-8138.12101
Conflict of interest: none.
- Issue published online: 14 MAY 2013
- Article first published online: 27 FEB 2013
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