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Ito, Yoko, Carss, Keren J, Duarte, Sofia T, Hartley, Taila, Keren, Boris, Kurian, Manju A, Marey, Isabelle, Charles, Perinne, Mendonça, Carla 
ORCID: 0000-0001-9926-0598, Nava, Caroline et al (show 11 more authors)
(2018)
De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures.
American journal of human genetics, 103 (1).
144 - 153.
Kirschner, Kristina, Samarajiwa, Shamith A, Cairns, Jonathan M, Menon, Suraj, Perez-Mancera, Pedro A, Tomimatsu, Kosuke, Bermejo-Rodriguez, Camino, Ito, Yoko, Chandra, Tamir, Narita, Masako et al (show 6 more authors)
(2015)
Phenotype Specific Analyses Reveal Distinct Regulatory Mechanism for Chronically Activated p53.
PLOS GENETICS, 11 (3).