Comment on

• A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns.

  Singh NA, Charlier C, Stauffer D, DuPont BR, Leach RJ, Melis R, Ronen GM, Bjerre I, Quattlebaum T, Murphy JV, McHarg ML, Gagnon D, Rosales TO, Peiffer A, Anderson VE, Leppert M. Singh NA, et al. Nat Genet. 1998 Jan;18(1):25-9. doi: 10.1038/ng0198-25. Nat Genet. 1998. PMID: 9425895
• A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family.

  Charlier C, Singh NA, Ryan SG, Lewis TB, Reus BE, Leach RJ, Leppert M. Charlier C, et al. Nat Genet. 1998 Jan;18(1):53-5. doi: 10.1038/ng0198-53. Nat Genet. 1998. PMID: 9425900