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Molecular analysis of mutations in the CSB (ERCC6) gene in patients with Cockayne syndrome.

Cockayne syndrome is a multisystem sun-sensitive genetic disorder associated with a specific defect in the ability to perform transcription-coupled repair of active genes after UV irradiation. Two complementation groups (CS-A and CS-B) have been identified, and 80% of patients have been assigned to...

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Detalhes bibliográficos
Main Authors: Mallery, D L, Tanganelli, B, Colella, S, Steingrimsdottir, H, van Gool, A J, Troelstra, C, Stefanini, M, Lehmann, A R
Formato: Artigo
Idioma:Inglês
Publicado em: 1998
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1376810/
https://ncbi.nlm.nih.gov/pubmed/9443879
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