Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome...

GH Ashton, WH McLean, AP South, N Oyama, FJ Smith, R Al-Suwaid, A Al-Ismaily, DJ Atherton, CA Harwood, IM Leigh, Celia Moss, B Didona, G Zambruno, A Patrizi, RA Eady, JA McGrath

Research output: Contribution to journalArticle

77 Citations (Scopus)
Original languageEnglish
Pages (from-to)78-83
Number of pages6
JournalJournal of Investigative Dermatology
Publication statusPublished - 1 Jan 2004

Cite this