Publication: Novel germline ERCC5 mutations identified in a xeroderma pigmentosum complementation group G pedigree
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Date
2015
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Elsevier
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Wang, Tao, Chen-chen Xu, Xi-ping Zhou, Jonathan J. Lee, Jun Shen, Bill Q. Lian, Yue-Hua Liu, and Christine Guo Lian. 2015. “Novel germline ERCC5 mutations identified in a xeroderma pigmentosum complementation group G pedigree.” JAAD Case Reports 1 (2): 66-70. doi:10.1016/j.jdcr.2014.12.004. http://dx.doi.org/10.1016/j.jdcr.2014.12.004.
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, Excision Repair Cross-complementing Rodent Repair Deficiency Complementation Group 5 gene, nucleotide excision repair, whole exome sequencing, xeroderma pigmentosum complementation group G, CS, Cockayne syndrome, NER, Nucleotide excision repair, UV, Ultraviolet, WES, Whole exome sequencing, XP, Xeroderma pigmentosum, XP-G, Xeroderma pigmentosum complementation group G
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