A GENE AND MUTATIONS THEREOF ASSOCIATED WITH SEIZURE AND MOVEMENT DISORDERS

The present invention relates to the proline rich transmembrane protein 2 (PRRT2) gene, and the identification of mutations and variations in PRRT2 that give rise to seizure and movement disorders. Accordingly, the present invention provides methods for the diagnosis or prognosis of such disorders b...

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Bibliographische Detailangaben
Hauptverfasser: SCHEFFER, INGRID, EILEEN, MULLEY, JOHN, CHARLES, HERON, SARAH, ELIZABETH, BERKOVIC, SAMUEL, FRANK, DIBBENS, LEANNE, MICHELLE
Format: Patent
Sprache:eng ; fre
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