Associated Papers
Report of a Novel Homozygous Intragenic DCC Duplication and a Review of Literature of Developmental Split-Brain Syndrome aka Horizontal Gaze Palsy with Progressive Scoliosis-2 with Impaired Intellectual Development Syndrome.
Rahikkala E et al.
Molecular Syndromology, 2024
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
A novel homozygous frameshift mutation in the DCC gene in a Pakistani family with autosomal recessive horizontal gaze palsy with progressive scoliosis-2 with impaired intellectual development.
Zaka A et al.
American Journal of Medical Genetics. Part A, 2021
DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome.
Marsh APL et al.
Human Mutation, 2018
Biallelic mutations in human DCC cause developmental split-brain syndrome.
Jamuar SS et al.
Nature Genetics, 2017
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