Neyroud N.,1999
Neyroud N., Richard P., Vignier N., Donger C., Denjoy I., Demay L., Shkolnikova M., Perse R., Chevalier P., Hainque B., Coumel P., Schwartz K., Guicheney P. Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in theLong QT syndrome. Circ.Res., 1999, v. 84, p. 290-297.
