Exome sequencing identified rare recurrent copy number variants and hereditary breast cancer susceptibility. Kumpula TA, Vorimo S, Mattila TT, O'Gorman L, et al. PLoS Genet 2023;19:e1010889.

Read + Share

Amedeo Smart

Independent Medical Education

Read + Share

Kumpula TA, Vorimo S, Mattila TT, O'Gorman L, et al. Exome sequencing identified rare recurrent copy number variants and hereditary breast cancer susceptibility. PLoS Genet 2023;19:e1010889.
PMID: 37578974