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Por Kelland, E., Rupar, C.A., Prasad, Asuri N., Tay, K.Y., Downie, A., Prasad, C.
Publicado no Mol Genet Metab Rep (2016)
Obter o texto integralPublicado no Mol Genet Metab Rep (2016)
Obter o texto integral
Obter o texto integral
Artigo
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Heterozygous De Novo UBTF Gain-of-Function Variant Is Associated with Neurodegeneration in Childhood
Por Edvardson, Simon, Nicolae, Claudia M., Agrawal, Pankaj B., Mignot, Cyril, Payne, Katelyn, Prasad, Asuri Narayan, Prasad, Chitra, Sadler, Laurie, Nava, Caroline, Mullen, Thomas E., Begtrup, Amber, Baskin, Berivan, Powis, Zöe, Shaag, Avraham, Keren, Boris, Moldovan, George-Lucian, Elpeleg, Orly
Publicado no Am J Hum Genet (2017)
Obter o texto integralPublicado no Am J Hum Genet (2017)
Obter o texto integral
Obter o texto integral
Artigo
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Por Scharfman, Helen E., Kanner, Andres M., Friedman, Alon, Blumcke, Ingmar, Crocker, Candice E., Cendes, Fernando, Diaz-Arrastia, Ramon, Förstl, Hans, Fenton, André A., Grace, Anthony A., Palop, Jorge, Morrison, Jason, Nehlig, Astrid, Prasad, Asuri, Wilcox, Karen S., Jette, Nathalie, Pohlmann-Eden, Bernd
Publicado no Epilepsy Behav (2017)
Obter o texto integralPublicado no Epilepsy Behav (2017)
Obter o texto integral
Obter o texto integral
Artigo