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A new keratin 5 mutation (K199T) in a family with Weber–Cockayne epidermolysis bullosa simplex

✍ Scribed by Z. Xu; H. Dong; X. Sun; X. Zhu; Y. Yang


Book ID
108692436
Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
90 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][