Results
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N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratoderma by
- Rickman, L
- 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, D
Material type:  Text; Format:
print ; Literary form:
Not fiction
In: Human Molecular Genetics 8 (6), 971-976.
Availability: Items available for loan: Staff publications (1)Call number: XX(10545.1).
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Striate palmoplantar keratoderma arising from desmoplakin and desmoglein 1 mutations is associated with contrasting perturbations of desmosomes and the keratin filament network by
- Wan, H
- Armstrong, D. K. B
- Buxton, R. S
- Dopping-Hepenstal, P. J. C
- Eady, R. A. J
- Gratian, M. J
- Keane, F
- McGrath, J. A
- Purkis, P. E
- South, A. P
- Stone, M. G
- Zhu, G
Material type: Text; Format:
print ; Literary form:
Not fiction
In: British Journal of Dermatology 150 (5), 878-891.
Availability: Items available for loan: Staff publications (1)Call number: XX(12827.1).
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