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A keratin 14 'knockout' mutation in recessive epidermolysis bullosa simplex resulting in less severe disease. [electronic resource] by
- Batta, K
- Rugg, E L
- Wilson, N J
- West, N
- Goodyear, H
- Lane, E B
- Gratian, M
- Dopping-Hepenstal, P
- Moss, C
- Eady, R A
Producer: 20001024
In:
The British journal of dermatology vol. 143
Availability: No items available.
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17.
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Psoriasis bullosa acquisita. [electronic resource] by
- Morris, S D
- Mallipeddi, R
- Oyama, N
- Gratian, M J
- Harman, K E
- Bhogal, B S
- Black, M M
- Eady, R A J
- Hashimoto, T
- McGrath, J A
Producer: 20030319
In:
Clinical and experimental dermatology vol. 27
Availability: No items available.
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18.
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Homozygous nonsense mutation in helix 2 of K14 causes severe recessive epidermolysis bullosa simplex. [electronic resource] by
- Corden, L D
- Mellerio, J E
- Gratian, M J
- Eady, R A
- Harper, J I
- Lacour, M
- Magee, G
- Lane, E B
- McGrath, J A
- McLean, W H
Producer: 19980604
In:
Human mutation vol. 11
Availability: No items available.
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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. [electronic resource] by
- Wan, H
- Dopping-Hepenstal, P J C
- Gratian, M J
- Stone, M G
- Zhu, G
- Purkis, P E
- South, A P
- Keane, F
- Armstrong, D K B
- Buxton, R S
- McGrath, J A
- Eady, R A J
Producer: 20040715
In:
The British journal of dermatology vol. 150
Availability: No items available.
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