Clinical classification of BRCA1 DNA missense variants: H1686Q is a novel pathogenic mutation occurring in the ontogenetically invariant THV motif of the N-terminal BRCT domain

Giuseppe Giannini, Carlo Capalbo, Laura Ottini, Amelia Buffone, Laura De Marchis, Elena Margaria, Domenico Vitolo, Enrico Ricevuto, Christian Rinaldi, Massimo Zani, Sergio Ferraro, Paolo Marchetti, Enrico Cortesi, Luigi Frati, Isabella Screpanti, Alberto Gulino

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)4212-4214
Number of pages3
JournalJournal of Clinical Oncology
Volume26
Issue number25
DOIs
Publication statusPublished - 2008

ASJC Scopus subject areas

  • Cancer Research
  • Oncology

Cite this

Giannini, G., Capalbo, C., Ottini, L., Buffone, A., De Marchis, L., Margaria, E., Vitolo, D., Ricevuto, E., Rinaldi, C., Zani, M., Ferraro, S., Marchetti, P., Cortesi, E., Frati, L., Screpanti, I., & Gulino, A. (2008). Clinical classification of BRCA1 DNA missense variants: H1686Q is a novel pathogenic mutation occurring in the ontogenetically invariant THV motif of the N-terminal BRCT domain. Journal of Clinical Oncology, 26(25), 4212-4214. https://doi.org/10.1200/JCO.2008.18.2089