Founder mutation c.676insC in three unrelated kindler syndrome families belonging to a particular clan from Pakistan.

Shaiq, P. A., Klausegger, A., Muzzaffar, F., Latif, A., Bauer, J. W., Imran, M., Khanum, A., Qamar R. and Raja G. K.  The Journal of Dermatology,  39:640-641 (2012).