Identification of Two Missense Mutations of ERCC6 in Three Chinese Sisters with Cockayne Syndrome by Whole Exome Sequencing

Cockayne syndrome (CS) is a rare autosomal recessive disorder, the primary manifestations of which are poor growth and neurologic abnormality. Mutations of the ERCC6 and ERCC8 genes are the predominant cause of Cockayne syndrome, and the ERCC6 gene mutation is present in approximately 65% of cases....

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Detalles Bibliográficos
Autores principales: Yu, Shanshan, Chen, Liyuan, Ye, Lili, Fei, Lingna, Tang, Wei, Tian, Yujiao, Geng, Qian, Yi, Xin, Xie, Jiansheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4252064/
https://www.ncbi.nlm.nih.gov/pubmed/25463447
http://dx.doi.org/10.1371/journal.pone.0113914

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4252064/
https://www.ncbi.nlm.nih.gov/pubmed/25463447
http://dx.doi.org/10.1371/journal.pone.0113914

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