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
Induction of senescence pathways in Kindler syndrome primary keratinocytes.
Piccinni E et al.
The British Journal of Dermatology, 2013
Kindler syndrome: extension of FERMT1 mutational spectrum and natural history.
Has C et al.
Human Mutation, 2011
[Kindler syndrome. A new bullous dermatosis].
Has C
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete, 2009
Kindler syndrome: a focal adhesion genodermatosis.
Lai-Cheong JE et al.
The British Journal of Dermatology, 2009
A novel frameshift mutation in the KIND1 gene in Turkish siblings with Kindler syndrome.
Kaçar N et al.
The British Journal of Dermatology, 2008
Five new homozygous mutations in the KIND1 gene in Kindler syndrome.
Lai-Cheong JE et al.
The Journal of Investigative Dermatology, 2007
Molecular basis of Kindler syndrome in Italy: novel and recurrent Alu/Alu recombination, splice site, nonsense, and frameshift mutations in the KIND1 gene.
Has C et al.
The Journal of Investigative Dermatology, 2006
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