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Mutation of human keratin 18 in association with cryptogenic cirrhosis.

Mutations in 11 of the more than 20 keratin intermediate filaments cause several epidermal and oral associated diseases. No disease-associated mutations have been described in keratin 8 or 18 (K8/18) which are the major keratin pair in simple-type epithelia, as found in the liver, pancreas, and inte...

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Detalles Bibliográficos
Main Authors: Ku, N O, Wright, T L, Terrault, N A, Gish, R, Omary, M B
Formato: Artigo
Idioma:Inglês
Publicado: 1997
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC507762/
https://ncbi.nlm.nih.gov/pubmed/9011570
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