Tyson J.,1997b
Tyson J., Tranebjaerg L., Bellman S., Wren C., Taylor J., Bathen J., Aslaksen B., Sorland S.J., Lund O., Malcolm S., Pembrey M., Bhattacharya S., Bitner-Glindzicz M. IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause the Jervell and Lange-Nielsen syndrome. - Hum.Mol.Genet., 1997, v. 6, p. 2179-2185.
