Comment on

• Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.

  Lee MP, Hu RJ, Johnson LA, Feinberg AP. Lee MP, et al. Nat Genet. 1997 Feb;15(2):181-5. doi: 10.1038/ng0297-181. Nat Genet. 1997. PMID: 9020845
• A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome.

  Neyroud N, Tesson F, Denjoy I, Leibovici M, Donger C, Barhanin J, Fauré S, Gary F, Coumel P, Petit C, Schwartz K, Guicheney P. Neyroud N, et al. Nat Genet. 1997 Feb;15(2):186-9. doi: 10.1038/ng0297-186. Nat Genet. 1997. PMID: 9020846