Kindlin-1 protein-protein interactions and functional relevance to Kindler syndrome
Kindler syndrome (KS) is an autosomal recessive genodermatosis resulting from pathogenic mutations in the FERMT1 (KIND) gene. This gene encodes kindlin-1 (also known as fermitin family homologue 1), a focal adhesion protein involved in activation of the integrin family of extracellular matrix recept...
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King's College London (University of London)
2013
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| Online Access: | https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.762262 |