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Precision screening facilitates clinical classification of BRCA2-PALB2 binding variants with benign and pathogenic functional effects

BACKGROUND Decoding the clinical impact of genetic variants is particularly important for precision medicine in cancer. Genetic screening of mainly patients with breast and ovarian cancer has identified numerous BRCA1/BRCA2 variants of uncertain significance (VUS) that remain unclassified owing to a...

Бүрэн тодорхойлолт

-д хадгалсан:
Номзүйн дэлгэрэнгүй
Үндсэн зохиолчид: Muthiah Bose, Manika Indrajit Singh, Morten Frödin, Bent Ejlertsen, Claus S. Sørensen, Maria Rossing
Формат: Artigo
Хэл сонгох:Inglês
Хэвлэсэн: American Society for Clinical Investigation 2025-06-01
Цуврал:The Journal of Clinical Investigation
Нөхцлүүд:
Онлайн хандалт:https://doi.org/10.1172/JCI181879
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