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P3.1 Clinical and neurophysiological features of progressive myoclonus epilepsy associated with SCARB2 mutations without renal failure

✍ Scribed by G. Rubboli; S. Franceschetti; S.F. Berkovic; L. Canafoglia; A. Gambardella; L.M. Dibbens; P. Riguzzi; C. Campieri; A. Magaudda; C.A. Tassinari; R. Michelucci

Book ID: 117773914
Publisher: Elsevier Science
Year: 2011
Tongue: English
Weight: 41 KB
Volume: 122
Category: Article
ISSN: 1388-2457
DOI: 10.1016/s1388-2457(11)60220-4

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