Weber, Y. Et Al. 2012. PRRT2 MUTATIONS ARE THE MAJOR CAUSE OF BENIGN FAMILIAL INFANTILE SEIZURES (BFIS). 10th European Congress on Epileptology , (London, Canada), 2.

Weber, Y., Schubert, J., Paravidino, R., Becker, F., Berger, A., Bebek, N., ... Bianchi, A.(2012). PRRT2 MUTATIONS ARE THE MAJOR CAUSE OF BENIGN FAMILIAL INFANTILE SEIZURES (BFIS) . 10th European Congress on Epileptology (pp.2). London, Canada

Weber, Y. Et Al. "PRRT2 MUTATIONS ARE THE MAJOR CAUSE OF BENIGN FAMILIAL INFANTILE SEIZURES (BFIS)," 10th European Congress on Epileptology, London, Canada, 2012

Weber, Y. Et Al. "PRRT2 MUTATIONS ARE THE MAJOR CAUSE OF BENIGN FAMILIAL INFANTILE SEIZURES (BFIS)." 10th European Congress on Epileptology , London, Canada, pp.2, 2012

Weber, Y. Et Al. (2012) . "PRRT2 MUTATIONS ARE THE MAJOR CAUSE OF BENIGN FAMILIAL INFANTILE SEIZURES (BFIS)." 10th European Congress on Epileptology , London, Canada, p.2.

@conferencepaper{conferencepaper, author={Y. Weber Et Al. }, title={PRRT2 MUTATIONS ARE THE MAJOR CAUSE OF BENIGN FAMILIAL INFANTILE SEIZURES (BFIS)}, congress name={10th European Congress on Epileptology}, city={London}, country={Canada}, year={2012}, pages={2} }