N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratoderma

By: Rickman, LContributor(s): Arnemann, J | Bryant, S. P | Buxton, R. S | Eady, R. A. J | Hunt, D. M | Kelsell, D. P | King, I. A | Leigh, I. M | Magee, A. I | Stevens, H. P | Šimrak, DMaterial type: TextTextReference number:PUB10420 In: Human Molecular Genetics 8 (6), 971-976.
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Magazine Magazine Staff publications New Materials Shelf Non-fiction XX(10545.1) (Browse shelf(Opens below)) 1 Available 10545-1001
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