Association of a common complement receptor 2 haplotype with increased risk of systemic lupus erythematosus

A genomic region on distal mouse chromosome 1 and its syntenic human counterpart 1q23–42 show strong evidence of harboring lupus susceptibility genes. We found evidence of linkage at 1q32.2 in a targeted genome scan of 1q21–43 in 126 lupus multiplex families containing 151 affected sibpairs (nonpara...

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Autors principals: Wu, Hui, Boackle, Susan A., Hanvivadhanakul, Punchong, Ulgiati, Daniela, Grossman, Jennifer M., Lee, Youngho, Shen, Nan, Abraham, Lawrence J., Mercer, Timothy R., Park, Elly, Hebert, Lee A., Rovin, Brad H., Birmingham, Dan J., Chang, Deh-Ming, Chen, Chung Jen, McCurdy, Deborah, Badsha, Humeira M., Thong, Bernard Y. H., Chng, Hiok H., Arnett, Frank C., Wallace, Daniel J., Yu, C. Yung, Hahn, Bevra H., Cantor, Rita M., Tsao, Betty P.
Format: Artigo
Idioma:Inglês
Publicat: National Academy of Sciences 2007
Matèries:
Biological Sciences
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1820691/
https://ncbi.nlm.nih.gov/pubmed/17360460
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0609101104
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