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Lehalle D, Mizuguchi T, Nava C, Matsumoto N, Cope H, de Man S, Friedman J, Joset P, Kato M, Muffels I, Nakamura K, Person RE, Petit F, Rauch A, Shashi V, Smol T, Steindl K, Torti E, Van de Laar I, Fuchs S, Depienne C, Mignot C. Further evidence to link CHD family-chromatin remodeler genes and neurodevelopment: de novo variants in CHD5 are associated with intellectual disability, epilepsy and autism. EUROPEAN JOURNAL OF HUMAN GENETICS. 2020. p. 326–327.