Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratoderma

By: Hunt, D. MContributor(s): Armstrong, D. K. B | Arnemann, J | Buxton, R. S | Dopping-Hepenstal, P. J. C | Eady, R. A | Hennies, H. C | Hughes, A. E | Kelsell, D. P | Kuster, W | Leigh, I. M | McGrath, J. A | Rickman, L | Simrak, D | Stevens, H. P | Whittock, N. VMaterial type: TextTextReference number:PUB10999 In: European Journal of Human Genetics 9 (3), 197-203.
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Item type Current library Collection Class number Copy number Status Date due Barcode Item reservations
Magazine Magazine Staff publications New Materials Shelf Non-fiction XX(11098.1) (Browse shelf(Opens below)) 1 Available 11098-1001
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