Related references
Note: Only part of the references are listed.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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Neurotransmitter trafficking defect in a patient with clathrin (CLTC) variation presenting with intellectual disability and early-onset parkinsonism
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High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies
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AMERICAN JOURNAL OF HUMAN GENETICS (2017)
CLTC as a clinically novel gene associated with multiple malformations and developmental delay
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AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2016)
Clathrin light chains are required for the gyrating-clathrin recycling pathway and thereby promote cell migration
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NATURE COMMUNICATIONS (2014)