Associated Papers
Characterization of Amino Acid Substitutions and Deletions in Kindlin-1 FERM Domain: Relevance for Precision Medicine.
Yilmaz P et al.
The Journal of Investigative Dermatology, 2022
Fibroblast activation and abnormal extracellular matrix remodelling as common hallmarks in three cancer-prone genodermatoses.
Chacón-Solano E et al.
The British Journal of Dermatology, 2019
Oxidative stress and mitochondrial dysfunction in Kindler syndrome.
Zapatero-Solana E et al.
Orphanet Journal of Rare Diseases, 2014
Kindler syndrome: extension of FERMT1 mutational spectrum and natural history.
Has C et al.
Human Mutation, 2011
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