Associated Papers
High-throughput mapping of 6,888 RAD51D variants identifies distinct biochemical functions needed for homologous recombination and olaparib response.
Darrah KE et al.
Biorxiv : the Preprint Server for Biology, 2026
41542474 (PubMed )
Supplement: media-1.xlsx › Sup._Table_5_MAVE_SNVs_
Congenital Mirror Movements Due to RAD51: Cosegregation with a Nonsense Mutation in a Norwegian Pedigree and Review of the Literature.
Trouillard O et al.
Tremor and Other Hyperkinetic Movements (new York, N.y.), 2016
Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.
Méneret A et al.
Neurology, 2014
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