Number of items: 1.
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McCormack, Mark, Gui, Hongsheng, Ingason, Andres, Speed, Doug, Wright, Galen EB, Zhang, Eunice J, Secolin, Rodrigo, Yasuda, Clarissa, Kwok, Maxwell, Wolking, Stefan et al (show 43 more authors) , Becker, Felicitas, Rau, Sarah, Avbersek, Andreja, Heggeli, Kristin, Leu, Costin, Depondt, Chantal, Sills, Graeme J ORCID: 0000-0002-3389-8713, Marson, Anthony G ORCID: 0000-0002-6861-8806, Auce, Pauls, Brodie, Martin J, Francis, Ben ORCID: 0000-0002-2130-5976, Johnson, Michael R, Koeleman, Bobby PC, Striano, Pasquale, Coppola, Antonietta, Zara, Federico, Kunz, Wolfram S, Sander, Josemir W, Lerche, Holger, Klein, Karl Martin, Weckhuysen, Sarah, Krenn, Martin, Gudmundsson, Larus J, Stefansson, Kari, Krause, Roland, Shear, Neil, Ross, Colin JD, Delanty, Norman, Pirmohamed, Munir ORCID: 0000-0002-7534-7266, Carleton, Bruce C, Cendes, Fernando, Lopes-Cendes, Iscia, Liao, Wei-ping, O'Brien, Terence J, Sisodiya, Sanjay M, Cherny, Stacey, Kwan, Patrick, Baum, Larry, Cavalleri, Gianpiero L, Consortium, EPIGEN, Network, Canadian Pharmacogenomics, Consortium, for the EpiPGX and Consortium, Int League Epilepsy
(2018)
Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients.
NEUROLOGY, 90 (4).
E332 - +.
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