Associated Papers
Assessment of the risk and characterization of non-melanoma skin cancer in Kindler syndrome: study of a series of 91 patients.
Guerrero-Aspizua S et al.
Orphanet Journal of Rare Diseases, 2019
Kindler syndrome: extension of FERMT1 mutational spectrum and natural history.
Has C et al.
Human Mutation, 2011
Novel and recurrent FERMT1 gene mutations in Kindler syndrome.
Techanukul T et al.
Acta Dermato-venereologica, 2011
Kindlin-1 Is required for RhoGTPase-mediated lamellipodia formation in keratinocytes.
Has C et al.
The American Journal of Pathology, 2009
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