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We ignore the low probability event of an apparent coincident mutation arising from lineage sorting and require that multiple mutations be used to explain the observed data.
In contrast, the LT gene in case AC43 had a frameshift mutation arising from a 46-base pair (bp) deletion at nt positions 1611 1656, which generated several stop codons.
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Next, we ruled out a possibility that the large effect of the H1061N mutation arose from a perturbation of oligomerization.
Furthermore, in the particular case of Slo2.2, it has been proposed that severe human pathologies associated with Slo2.2 mutation arise from extensive alterations in gene and protein expression throughout the nervous system (Kaczmarek, 2013).
The reference sequence I161, G265, F330 and G368 (allele IGFG) most probably represents the wild type sequence since then same amino-acids were present in the other available AChE sequences from Brachycera (Musca domestica, Lucilia cuprina and Bractrocera oleae) and each mutation arose from a single mutation.
38 Azizan et al suggested that APAs with a somatic KCNJ5 mutation arise from ZF cells, even though the possibility that cytological features and modifications were due to the effect of the mutation on ZG-derived cells could not be ruled out.
The elucidation of the DNA structure provided the essential foundation for defining the different types of mutations arising from both spontaneous and environmental DNA damage that affect all living cells12.
The possibility of falsely elevating the rate of TDR by separately counting TDR mutations arising from a single specimen was addressed in this study.
To provide insights into the physiological role of PiT1 in mice, we established an allelic series of PiT1 mutations arising from the combination of normal, hypomorphic and null PiT1 alleles in mice.
Since the 2007 list was published, new drug-resistance mutations have been identified including mutations arising from the increased use of non-thymidine-analog containing regimens, the expanded use of two new protease inhibitors (PIs), and the recent approval of a new non-nucleoside RT inhibitor (NNRTI).
While many methods are available for detecting dominant SNPs, a simple multiplex platform to detect minority variants might offer greater information yield and could be used for a broader scope of applications such as detecting SNPs implicated in somatic cell carcinogenesis [4] or identifying drug resistance mutations arising from pathogen or cancer chemotherapy [5].
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