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The prevalence of the pfmdr1 86Y mutation was higher after treatment with AQ+SP than after SP, p = 0.002.
At the post-intervention survey, the proportion of parasitaemic children carrying parasites with the dhfr triple mutation and the dhps mutation was higher in children in the SP+AS arm than in the placebo arm (dhfr: SP+AS 95%, placebo 75%, p = 0.01 and dhps: SP+AS 86%, placebo 44%, p<0.001).
Also, the frequency of mutation was higher in exon 2 than exon 1 (3 cases in exon 2 compared with 1 case for exon 1).
In this study, we demonstrated that frequency of KRAS mutation was higher in LST-G than in LST-NG or polypid tumors.
The incidence of the EGFR driver mutation was higher in Asian NSCLC; 32% in Asians while 7% in non-Asians (Mitsudomi and Yatabe, 2007).
The frequency of the exon 3 T to C mutation was higher in cancer patients than in controls (odds ratio 3.8; 95% confidence intervals 1.8 8.0).
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Frequency of L1014S point mutation was high for An.
In our study of patients with advanced disease, the serum ferritin cutoff for the diagnosis of HFE-HH mutation was high at 2,685 ng/mL.
The prevalence of KRAS mutation is higher than that in recent molecular studies [ 21, 24].
We find that EGFR is overexpressed and the risk of having BRCA1 mutation is higher in TNBC than non-TNBC.
For example, the K-ras gene mutation is higher in Caucasian NSCLC patients than in Asian NSCLC patients.
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