Ackerman M.J.,1998
Ackerman M.J., Schroeder J.J., Berry R., Schaid D.J., Porter C.B., Michels V.V., Thibodeau S.N. A novel mutation in KVLQT1 is the molecular basis of inherited long QT syndrome in a near-drowning patient's family. - Pediat.Res., 1998, v. 44, p. 148- 153.
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