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A new mutation in the linker 12 domain of keratin 5 in a Chinese family with Weber–Cockayne epidermolysis bullosa simplex

✍ Scribed by J.-G. Li; J. Feng; S.-X. Xiao; Y.-L. Ai; J.-M. Wang; Z.-H. Peng


Book ID
108692556
Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
147 KB
Volume
29
Category
Article
ISSN
0307-6938

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## Communicated by Darwin J. Prockop We have previously reported linkage of a large Finnish family with the generalized (Kobner) type of epidermolysis bullosa simplex to chromosome 12q in the region containing the type I1 keratin gene cluster (Ryynanen et al., Am J Human Genet 49: [978][979][980][