Wird geladen...
Design and validation of a next generation sequencing assay for hereditary BRCA1 and BRCA2 mutation testing
Hereditary breast and ovarian cancer syndrome, caused by a germline pathogenic variant in the BRCA1 or BRCA2 (BRCA1/2) genes, is characterized by an increased risk for breast, ovarian, pancreatic and other cancers. Identification of those who have a BRCA1/2 mutation is important so that they can tak...
Gespeichert in:
| Veröffentlicht in: | PeerJ |
|---|---|
| Hauptverfasser: | , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
PeerJ Inc.
2016
|
| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4928470/ https://ncbi.nlm.nih.gov/pubmed/27375968 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7717/peerj.2162 |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|