Structure of the Highly Conserved HERC2 Gene and of Multiple Partially Duplicated Paralogs in Human

Recombination between chromosome-specific low-copy repeats (duplicons) is an underlying mechanism for several genetic disorders. Recently, a chromosome 15 duplicon was discovered in the common breakpoint regions of Prader–Willi and Angelman syndrome deletions. We identified previously the large HERC...

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Vydáno v:	Genome Res
Hlavní autoři:	Ji, Yonggang, Rebert, Nancy A., Joslin, John M., Higgins, Michael J., Schultz, Roger A., Nicholls, Robert D.
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Cold Spring Harbor Laboratory Press 2000
Témata:	Letter
On-line přístup:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC311424/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10720573/ https://ncbi.nlm.nih.govhttps://doi.org/10.1101/gr.10.3.319
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