PRRT2 Mutations Are the Major Cause of Benign Familial Infantile Seizures

DSpace Repository

PRRT2 Mutations Are the Major Cause of Benign Familial Infantile Seizures

Author: Schubert, Julian; Paravidino, Roberta; Becker, Felicitas; Berger, Andrea; Bebek, Nerses; Bianchi, Amedeo; Brockmann, Knut; Capovilla, Giuseppe; Bernardina, Bernardo Dalla; Fukuyama, Yukio; Hoffmann, Georg F.; Jurkat-Rott, Karin; Anttonen, Anna-Kaisa; Kurlemann, Gerhard; Lehesjoki, Anna-Elina; Lehmann-Horn, Frank; Mastrangelo, Massimo; Mause, Ulrike; Mueller, Stephan; Neubauer, Bernd; Puest, 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; Weber, Yvonne G.
Tübinger Autor(en):
Schubert, Julian
Becker, Felicitas
Ruf, Susanne
Bauer, Peter
Lerche, Holger
Weber, Yvonne G.
Müller, Stephan
Schroeder, Christopher
Published in: Human Mutation (2012), Bd. 33, H. 10, S. 1439-1443
Verlagsangabe: Wiley - Blackwell
Language: English
Full text: http://dx.doi.org/10.1002/humu.22126
ISSN: 1059-7794
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Artikel
Show full item record

This item appears in the following Collection(s)