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In total, these three mutations plus a known recurrent mutation account for approximately 50% of all affected families, being 60% of BRCA1 and 30% of BRCA2 mutations recurrent.
Of these, exon 19 deletions and the exon 21 L858R point mutation account for more than 80% of mutations detected in tumors with EGFR mutations [ 2, 3].
Both recombination and mutation account for the r measure, whereas D′ is affected only by recombination, not mutational history (Weiss and Clark 2002; Carlson et al. 2004).
However, in clinical situations, carriers of BRCA mutation account for only a part of TNBC or basal-like breast cancer patients, so we also need to focus on the treatment of BRCA-proficient TNBC.
Together these mutation account for 88% of the 17p deletions positional candidate genes for the frequent allelic losses at 10q, 13q, and 17q are PTEN, BRCA2 and RB1, and BRCA1.
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The D469del mutation, used in this study, is the most common PSACH mutation accounting for approximately 30% of cases [34].
FHL5 with STXBP2 mutation accounts for only 6%, and no FHL4 patients have yet been found in Japan.
SOD1H46R mutation accounts for a mild form of familial ALS that was originally identified in Japanese kindred [32].
To prove the ΔCS mutation accounted for the accelerated loss of RGCs via the Fas receptor, we intercrossed ΔCS mice with Fas-deficient lpr mice.
KRAS mutation accounts for 86 % of all RAS mutations [ 26].
37 This same mutation accounts for 34% of Dutch cases.
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