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766.
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Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratoderma. [electronic resource] by
- Hunt, D M
- Rickman, L
- Whittock, N V
- Eady, R A
- Simrak, D
- Dopping-Hepenstal, P J
- Stevens, H P
- Armstrong, D K
- Hennies, H C
- Küster, W
- Hughes, A E
- Arnemann, J
- Leigh, I M
- McGrath, J A
- Kelsell, D P
- Buxton, R S
Producer: 20010621
In:
European journal of human genetics : EJHG vol. 9
Availability: No items available.
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