Associated Papers
The landscape of rare genetic variants in familial Waldenström macroglobulinemia.
Pemov A et al.
Blood Neoplasia, 2024
39036705 (PubMed )
Supplement: BNEO_NEO-2023-000111-mmc4.xlsx › Supplementary_Table_4
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
Biallelic mutations in human DCC cause developmental split-brain syndrome.
Jamuar SS et al.
Nature Genetics, 2017
Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.
Méneret A et al.
Neurology, 2014
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