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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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Dades bibliogràfiques
Publicat a:Genome Res
Autors principals: Ji, Yonggang, Rebert, Nancy A., Joslin, John M., Higgins, Michael J., Schultz, Roger A., Nicholls, Robert D.
Format: Artigo
Idioma:Inglês
Publicat: Cold Spring Harbor Laboratory Press 2000
Matèries:
Accés en línia: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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