Loss of imprinting of a paternally expressed transcript, with antisense orientation to K(V)LQT1, occurs frequently in Beckwith–Wiedemann syndrome and is independent of insulin-like growth factor II imprinting

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Detalhes bibliográficos
Publicado no:Proc Natl Acad Sci U S A
Main Authors: Lee, Maxwell P., DeBaun, Michael R., Mitsuya, Kohzoh, Galonek, Heidi L., Brandenburg, Sheri, Oshimura, Mitsuo, Feinberg, Andrew P.
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 1999
Assuntos:
Biological Sciences
Acesso em linha:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC21842/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10220444/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.96.9.5203
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