SCN1A duplications and deletions detected in Dravet...

SCN1A duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis

Carla Marini, Ingrid E. Scheffer, Rima Nabbout, Davide Mei, Kathy Cox, Leanne M. Dibbens, Jacinta M. McMahon, Xenia Iona, Rochio Sanchez Carpintero, Maurizio Elia, Maria Roberta Cilio, Nicola Specchio
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Volume:
50
Year:
2009
Language:
english
Pages:
9
DOI:
10.1111/j.1528-1167.2009.02013.x
File:
PDF, 178 KB
english, 2009
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