Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome. (Q34298513)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome. |
scientific article |
Statements
Recurrent mutations in kindlin-1, a novel keratinocyte focal contact protein, in the autosomal recessive skin fragility and photosensitivity disorder, Kindler syndrome (English)
Gabrielle H S Ashton
Andrew P South
Frances J D Smith
Raouf Al-Suwaid
Abla Al-Ismaily
David J Atherton
Irene M Leigh
Celia Moss
Biagio Didona
Giovanna Zambruno
Annalisa Patrizi
Robin A J Eady