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CLTC Research
Interested in Doing Research on CLTC-RD?
CLTC as a clinically novel gene associated with multiple malformations and developmental delay
Novel Mutation in CLTC Associated with Anomalous Development
Disorders Associated with CLTC Gene
De novo CLTC variants are associated with a variable phenotype from mild to severe intellectual disability, microcephaly, hypoplasia of the corpus callosum, and epilepsy
List of variants in gene CLTC studied for Intellectual disability
Evidence for CLTC in intellectual disability, autosomal dominant
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