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Recurrent and founder mutations in the netherlands: Mutation p.k217del in troponin t2, causing dilated cardiomyopathy

Otten, E. (Ellen), Lekanne Dit Deprez, R.H., Weiss, M.M. (Marjan), Slegtenhorst, M.A. (Marjon) van, Joosten, A-M.S (Marieke), Smagt, J.J. (Jasper) van der, Jonge, N. (Nicolaas) de, Kerstjense-Frederikse, W.S. (Wilhelmina), Roofthooft, M.T.R. (Marcus), Balk, A.H.M.M. (Aggie), Berg, M.P. (Maarten) van den, Ruiter, J.S., Tintelen, J.P. (Peter) van
2010