Nabais Sá, Maria J. http://orcid.org/0000-0002-2152-4626
Venselaar, Hanka
Wiel, Laurens
Trimouille, Aurélien
Lasseaux, Eulalie
Naudion, Sophie
Lacombe, Didier
Piton, Amélie
Vincent-Delorme, Catherine
Zweier, Christiane
Reis, André
Trollmann, Regina
Ruiz, Anna
Gabau, Elisabeth
Vetro, Annalisa
Guerrini, Renzo
Bakhtiari, Somayeh
Kruer, Michael C.
Amor, David J.
Cooper, Monica S.
Bijlsma, Emilia K.
Barakat, Tahsin Stefan
van Dooren, Marieke F.
van Slegtenhorst, Marjon
Pfundt, Rolph
Gilissen, Christian
Willemsen, Michèl A.
de Vries, Bert B.A.
de Brouwer, Arjan P.M.
Koolen, David A.
This article is maintained by: Elsevier
Article Title: De novo CLTC variants are associated with a variable phenotype from mild to severe intellectual disability, microcephaly, hypoplasia of the corpus callosum, and epilepsy
Journal Title: Genetics in Medicine
CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-019-0703-y
Content Type: article
Copyright: © 2020, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics