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.

Lee MP, DeBaun MR, Mitsuya K, Galonek HL, Brandenburg S, Oshimura M, Feinberg AP
Proc Natl Acad Sci U S A. 1999 96 (9): 5203-8

PMID: 10220444 · PMCID: PMC21842 · DOI:10.1073/pnas.96.9.5203

MeSH Terms (13)

Beckwith-Wiedemann Syndrome Chromosomes, Human, Pair 11 Gene Expression Regulation Genomic Imprinting Humans Insulin-Like Growth Factor II KCNQ1 Potassium Channel KCNQ Potassium Channels Membrane Proteins Potassium Channels Potassium Channels, Voltage-Gated Transcription, Genetic Wilms Tumor

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