Schubert, J. Et Al. 2012. PRRT2 Mutations Are the Major Cause of Benign Familial Infantile Seizures. HUMAN MUTATION , vol.33, no.10 , 1439-1443.

Schubert, J., Paravidino, R., Becker, F., Berger, A., Bebek, N., Bianchi, A., ... Brockmann, K.(2012). PRRT2 Mutations Are the Major Cause of Benign Familial Infantile Seizures. HUMAN MUTATION , vol.33, no.10, 1439-1443.

Schubert, Julian Et Al. "PRRT2 Mutations Are the Major Cause of Benign Familial Infantile Seizures," HUMAN MUTATION , vol.33, no.10, 1439-1443, 2012

Schubert, Julian Et Al. "PRRT2 Mutations Are the Major Cause of Benign Familial Infantile Seizures." HUMAN MUTATION , vol.33, no.10, pp.1439-1443, 2012

Schubert, J. Et Al. (2012) . "PRRT2 Mutations Are the Major Cause of Benign Familial Infantile Seizures." HUMAN MUTATION , vol.33, no.10, pp.1439-1443.

@article{article, author={Julian Schubert Et Al. }, title={PRRT2 Mutations Are the Major Cause of Benign Familial Infantile Seizures}, journal={HUMAN MUTATION}, year=2012, pages={1439-1443} }