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

G H S Ashton, W H I McLean, A P South, N Oyama, F J D Smith, R Al-Suwaid, A Al ismaily, D J Atherton, C A Harwood, I M Leigh, C Moss, B Didona, G Zambruno, A Patrizi, R A J Eady, J A McGrath

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Medicine and Dentistry

Biochemistry, Genetics and Molecular Biology