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.
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I. Screpanti | G. Giannini | E. Ricevuto | P. Marchetti | L. Ottini | L. Frati | A. Gulino | C. Capalbo | E. Cortesi | D. Vitolo | M. Zani | S. Ferraro | C. Rinaldi | Amelia Buffone | L. De Marchis | E. Margaria