APA
Schubert J., Paravidino R., Becker F., Berger A., Bebek N., Bianchi A., Brockmann K., Capovilla G., Dalla Bernardina B., Fukuyama Y., Hoffmann G. F., Jurkat-Rott K., Anttonen A., Kurlemann G., Lehesjoki A., Lehmann-Horn F., Mastrangelo M., Mause U., Müller S., Neubauer B., Püst B., Rating D., Robbiano A., Ruf S., Schroeder C., Seidel A., Specchio N., Stephani U., Striano P., Teichler J., Turkdogan D., Vigevano F., Viri M., Bauer P., Zara F., Lerche H. & Weber Y. G. (20130705). PRRT2 mutations are the major cause of benign familial infantile seizures. : Human mutation.
Chicago
Schubert Julian, Paravidino Roberta, Becker Felicitas, Berger Andrea, Bebek Nerses, Bianchi Amedeo, Brockmann Knut, Capovilla Giuseppe, Dalla Bernardina Bernardo, Fukuyama Yukio, Hoffmann Georg F, Jurkat-Rott Karin, Anttonen Anna-Kaisa, Kurlemann Gerhard, Lehesjoki Anna-Elina, Lehmann-Horn Frank, Mastrangelo Massimo, Mause Ulrike, Müller Stephan, Neubauer Bernd, Püst Burkhard, Rating Dietz, Robbiano Angela, Ruf Susanne, Schroeder Christopher, Seidel Andreas, Specchio Nicola, Stephani Ulrich, Striano Pasquale, Teichler Jens, Turkdogan Dilsad, Vigevano Federico, Viri Maurizio, Bauer Peter, Zara Federico, Lerche Holger and Weber Yvonne G. 20130705. PRRT2 mutations are the major cause of benign familial infantile seizures. : Human mutation.
Harvard
Schubert J., Paravidino R., Becker F., Berger A., Bebek N., Bianchi A., Brockmann K., Capovilla G., Dalla Bernardina B., Fukuyama Y., Hoffmann G. F., Jurkat-Rott K., Anttonen A., Kurlemann G., Lehesjoki A., Lehmann-Horn F., Mastrangelo M., Mause U., Müller S., Neubauer B., Püst B., Rating D., Robbiano A., Ruf S., Schroeder C., Seidel A., Specchio N., Stephani U., Striano P., Teichler J., Turkdogan D., Vigevano F., Viri M., Bauer P., Zara F., Lerche H. and Weber Y. G. (20130705). PRRT2 mutations are the major cause of benign familial infantile seizures. : Human mutation.
MLA
Schubert Julian, Paravidino Roberta, Becker Felicitas, Berger Andrea, Bebek Nerses, Bianchi Amedeo, Brockmann Knut, Capovilla Giuseppe, Dalla Bernardina Bernardo, Fukuyama Yukio, Hoffmann Georg F, Jurkat-Rott Karin, Anttonen Anna-Kaisa, Kurlemann Gerhard, Lehesjoki Anna-Elina, Lehmann-Horn Frank, Mastrangelo Massimo, Mause Ulrike, Müller Stephan, Neubauer Bernd, Püst Burkhard, Rating Dietz, Robbiano Angela, Ruf Susanne, Schroeder Christopher, Seidel Andreas, Specchio Nicola, Stephani Ulrich, Striano Pasquale, Teichler Jens, Turkdogan Dilsad, Vigevano Federico, Viri Maurizio, Bauer Peter, Zara Federico, Lerche Holger and Weber Yvonne G. PRRT2 mutations are the major cause of benign familial infantile seizures. : Human mutation. 20130705.