Variations in dysfunction of sister chromatid cohesion in esco2 mutant zebrafish reflect the phenotypic diversity of Roberts syndrome

Mutations in ESCO2, one of two establishment of cohesion factors necessary for proper sister chromatid cohesion (SCC), cause a spectrum of developmental defects in the autosomal-recessive disorder Roberts syndrome (RBS), warranting in vivo analysis of the consequence of cohesion dysfunction. Through...

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Detalles Bibliográficos
Autores principales: Percival, Stefanie M., Thomas, Holly R., Amsterdam, Adam, Carroll, Andrew J., Lees, Jacqueline A., Yost, H. Joseph, Parant, John M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4527282/
https://www.ncbi.nlm.nih.gov/pubmed/26044958
http://dx.doi.org/10.1242/dmm.019059

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4527282/
https://www.ncbi.nlm.nih.gov/pubmed/26044958
http://dx.doi.org/10.1242/dmm.019059

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