Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome.
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| Description | scientific article |
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author: Irwin McLean Catherine Harwood Noritaka Oyama John Mcgrath |
| Publication date | January 1, 2004 |
| Language | English |
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| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |