Two faces of the same coin: Benign familial infantile seizures and paroxysmal kinesigenic dyskinesia caused by PRRT2 mutations

Alexander Schmidt; Kishore R. Kumar; Katharina Redyk; Anne Grünewald; Matthias Leben; Alexander Münchau; Carolyn M. Sue; Johann Hagenah; Hans Hartmann; Katja Lohmann; Hans Jürgen Christen; Christine Klein

doi:10.1001/archneurol.2012.187

Two faces of the same coin: Benign familial infantile seizures and paroxysmal kinesigenic dyskinesia caused by PRRT2 mutations

Alexander Schmidt, Kishore R. Kumar, Katharina Redyk, Anne Grünewald, Matthias Leben, Alexander Münchau, Carolyn M. Sue, Johann Hagenah, Hans Hartmann, Katja Lohmann, Hans Jürgen Christen, Christine Klein^*

^*Corresponding author for this work

17 Citations (Scopus)

Original language	English
Journal	Archives of Neurology
Volume	69
Issue number	5
Pages (from-to)	668-670
Number of pages	3
ISSN	0003-9942
DOIs	https://doi.org/10.1001/archneurol.2012.187
Publication status	Published - 01.05.2012

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Schmidt, A., Kumar, K. R., Redyk, K., Grünewald, A., Leben, M., Münchau, A., Sue, C. M., Hagenah, J., Hartmann, H., Lohmann, K., Christen, H. J., & Klein, C. (2012). Two faces of the same coin: Benign familial infantile seizures and paroxysmal kinesigenic dyskinesia caused by PRRT2 mutations. Archives of Neurology, 69(5), 668-670. https://doi.org/10.1001/archneurol.2012.187

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Schmidt, A, Kumar, KR, Redyk, K, Grünewald, A, Leben, M, Münchau, A, Sue, CM, Hagenah, J, Hartmann, H, Lohmann, K, Christen, HJ & Klein, C 2012, 'Two faces of the same coin: Benign familial infantile seizures and paroxysmal kinesigenic dyskinesia caused by PRRT2 mutations', Archives of Neurology, vol. 69, no. 5, pp. 668-670. https://doi.org/10.1001/archneurol.2012.187

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AU - Schmidt, Alexander

AU - Kumar, Kishore R.

AU - Redyk, Katharina

AU - Grünewald, Anne

AU - Leben, Matthias

AU - Münchau, Alexander

AU - Sue, Carolyn M.

AU - Hagenah, Johann

AU - Hartmann, Hans

AU - Lohmann, Katja

AU - Christen, Hans Jürgen

AU - Klein, Christine

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Two faces of the same coin: Benign familial infantile seizures and paroxysmal kinesigenic dyskinesia caused by PRRT2 mutations

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