Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting.

Source:http://linkedlifedata.com/resource/pubmed/id/10220444

Proc. Natl. Acad. Sci. U.S.A. 1999 Apr 27 96 9 5203-8

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PMID
10220444