A novel mutation in LRSAM1 causes axonal Charcot-Marie-Tooth disease with dominant inheritance

Por Engeholm, Maik, Sekler, Julia, Schöndorf, David C, Arora, Vineet, Schittenhelm, Jens, Biskup, Saskia, Schell, Caroline, Gasser, Thomas
Publicado em 2014

Genome-scale networks link neurodegenerative disease genes to alpha-synuclein through specific molecular pathways

Por Khurana, Vikram, Peng, Jian, Chung, Chee Yeun, Auluck, Pavan K., Fanning, Saranna, Tardiff, Daniel F., Bartels, Theresa, Koeva, Martina, Eichhorn, Stephen W., Benyamini, Hadar, Lou, Yali, Nutter-Upham, Andy, Baru, Valeriya, Freyzon, Yelena, Tuncbag, Nurcan, Costanzo, Michael, Luis, Bryan-Joseph San, Schöndorf, David C., Barrasa, M. Inmaculada, Ehsani, Sepehr, Sanjana, Neville, Zhong, Quan, Gasser, Thomas, Bartel, David P., Vidal, Marc, Deleidi, Michela, Boone, Charles, Fraenkel, Ernest, Berger, Bonnie, Lindquist, Susan
Publicado no Cell Syst (2017)