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Paper Details

De novo CLTC variants are associated with a variable phenotype from mild to severe intellectual disability, microcephaly, hypoplasia of the corpus callosum, and epilepsy.
Genet Med
15
2020
Author NameAffiliation
Christian Gilissen
Bert B A de VriesDonders Institute for Brain, Radboud university medical center (Radboudumc)
David A KoolenDonders Institute for Brain, Radboud university medical center (Radboudumc)
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