SCN1A duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis von Marini, Carla, Scheffer, Ingrid E., Nabbout, Rima, Mei, Davide, Cox, Kathy, Dibbens, Leanne M., McMahon, Jacinta M., Iona, Xenia, Carpintero, Rochio Sanchez, Elia, Maurizio, Cilio, Maria Roberta, Specchio, Nicola, Giordano, Lucio, Striano, Pasquale, Gennaro, Elena, Cross, J. Helen, Kivity, Sara, Neufeld, Miriam Y., Afawi, Zaid, Andermann, Eva, Keene, Daniel, Dulac, Olivier, Zara, Federico, Berkovic, Samuel F., Guerrini, Renzo, Mulley, John C.

Volltext

SCNIA duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis von MARINI, Carla, SCHEFFER, Ingrid E, CILIO, Maria Roberta, SPECCHIO, Nicola, GIORDANO, Lucio, STRIANO, Pasquale, GENNARO, Elena, CROSS, J. Helen, KIVITY, Sara, NEUFELD, Miriam Y, AFAWI, Zaid, ANDERMANN, Eva, NABBOUT, Rima, KEENE, Daniel, DULAC, Olivier, ZARA, Federico, BERKOVIC, Samuel F, GUERRINI, Renzo, MULLEY, John C, MEI, Divide, COX, Kathy, DIBBENS, Leanne M, MCMAHON, Jacinta M, IONA, Xenia, SANCHEZ CARPINTERO, Rochio, ELIA, Maurizio

Volltext