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

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

scientific article

Author/s

author: Irwin McLean, Noritaka Oyama, Catherine Harwood, John McGrath

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Work details

Publication date

January 1, 2004

Language

English

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