Associated Papers
A novel heterozygous loss-of-function DCC Netrin 1 receptor variant in prenatal agenesis of corpus callosum and review of the literature.
Sagi-Dain L et al.
American Journal of Medical Genetics. Part A, 2020
DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome.
Marsh APL et al.
Human Mutation, 2018
Mutations in DCC cause congenital mirror movements.
Srour M et al.
Science (new York, N.y.), 2010
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