Phenotypes, genotypes and disease susceptibility associated with gene copy number variations: complement C4 CNVs in European American healthy subjects and those with systemic lupus erythematosus

A new paradigm in human genetics is high frequencies of inter-individual variations in copy numbers of specific genomic DNA segments. Such common copy number variation (CNV) loci often contain genes engaged in host-environment interaction including those involved in immune effector functions. DNA se...

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Autors principals: Wu, Y.L., Yang, Y., Chung, E.K., Zhou, B., Kitzmiller, K.J., Savelli, S.L., Nagaraja, H.N., Birmingham, D.J., Tsao, B.P., Rovin, B.H., Hebert, L.A., Yu, C.Y.
Format: Artigo
Idioma:Inglês
Publicat: S. Karger AG 2009
Matèries:
Copy Number Variation and Complex Disease
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2709077/
https://ncbi.nlm.nih.gov/pubmed/19287147
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000184700
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