Search Results - van Tintelen, Johan Peter

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    Phospholamban p.arg14del Mutation in a Spanish Family With Arrhythmogenic Cardiomyopathy: Evidence for a European Founder Mutation

    Phospholamban p.arg14del Mutation in a Spanish Family With Arrhythmogenic Cardiomyopathy: Evidence for a European Founder Mutation by López-Ayala, José María, Boven, Ludolf, van den Wijngaard, Arthur, Peñafiel-Verdú, Pablo, van Tintelen, Johan Peter, Gimeno, Juan Ramón

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    Phospholamban p.arg14del mutation in a Spanish family with arrhythmogenic cardiomyopathy: evidence for a European founder mutation

    Phospholamban p.arg14del mutation in a Spanish family with arrhythmogenic cardiomyopathy: evidence for a European founder mutation by López-Ayala, José María, Boven, Ludolf, van den Wijngaard, Arthur, Peñafiel-Verdú, Pablo, van Tintelen, Johan Peter, Gimeno, Juan Ramón

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    Severe Myocardial Fibrosis Caused by a Deletion of the 5’ End of the Lamin A/C Gene

    Severe Myocardial Fibrosis Caused by a Deletion of the 5’ End of the Lamin A/C Gene by van Tintelen, J. Peter, MD, Tio, Rene A., MD, PhD, Kerstjens-Frederikse, Wilhelmina S., MD, van Berlo, Jop H., MD, Boven, Ludolf G., BSc, Suurmeijer, Albert J.H., MD, PhD, White, Stefan J., PhD, den Dunnen, Johan T., PhD, te Meerman, Gerard J., PhD, Vos, Yvonne J., MSc, van der Hout, Annemarie H., PhD, Osinga, Jan, van den Berg, Maarten P., MD, PhD, van Veldhuisen, Dirk J., MD, PhD, Buys, Charles H.C.M., PhD, Hofstra, Robert M.W., PhD, Pinto, Yigal M., MD, PhD

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