De novo CLTC variants are associated with a variable phenotype from mild to severe intellectual disability, microcephaly, hypoplasia of the corpus callosum, and epilepsy
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| Description | scientific article published on 28 November 2019 |
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author: Renzo Guerrini Amélie Piton Tahsin Stefan Barakat David A Koolen |
| Publication date | November 28, 2019 |
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