Associated Papers
A large cohort study of prenatal exome sequencing redefines diagnosis in fetal corpus callosum anomalies.
Héron D et al.
Brain : a Journal of Neurology, 2025
40905141 (PubMed )
Supplement: awaf311_supplementary_data.zip › brain-2024-03287-File005.xlsx › Feuil1
Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected Individuals.
Collins Hutchinson ML et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2024
Novel DCC variants in congenital mirror movements and evaluation of disease-associated missense variants.
Bierhals T et al.
European Journal of Medical Genetics, 2018
DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome.
Marsh APL et al.
Human Mutation, 2018
Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.
Méneret A et al.
Neurology, 2014
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