Intraspecific Evolution of Human RCCX Copy Number Variation Traced by Haplotypes of the CYP21A2 Gene

The RCCX region is a complex, multiallelic, tandem copy number variation (CNV). Two complete genes, complement component 4 (C4) and steroid 21-hydroxylase (CYP21A2, formerly CYP21B), reside in its variable region. RCCX is prone to nonallelic homologous recombination (NAHR) such as unequal crossover,...

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Main Authors: Bánlaki, Zsófia, Szabó, Julianna Anna, Szilágyi, Ágnes, Patócs, Attila, Prohászka, Zoltán, Füst, George, Doleschall, Márton
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2013
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3595039/
https://ncbi.nlm.nih.gov/pubmed/23241443
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/gbe/evs121
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