Jongbloed R.J.E.,1999


Jongbloed R.J.E., Wilde A.A.M., Geelen J.L.M.C., Doevendans P., Schaap C., Van Langen I., Van Tintelen J.P., Cobben J.M., Beaufort-Krol G.C.M., Geraedts J.P.M., Smeets H.J.M. Novel KCNQ1 and HERG missense mutations in Dutch long-QT families. - Hum.Mut., 1999, v. 13, p. 301-310.

Смотрите также:

  • Синдром LQT2