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The patients with two class I, II, or III CFTR mutations were designated for group A (10 CF patients) and those with at least one class IV, V, or VI CFTR mutation were designated for group B (five CF patients).
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Subjects heterozygous or homozygous for the mutation are designated and subjects with the wild-type ALDH2 gene are designated.
Lack of a detectable C282Y or H63D mutation was designated as HFE wild-type (wt/wt).
The recombinant plasmids were checked by DNA sequencing, and the successfully introduced desired mutation was designated as pGEX-6p-I249L pGEX-6p-I249L pGEX-6p-I249L
In light of the phenotypic differences of this mutant with previously reported csgl1 (mict) and csgl2, this new mutation was designated as csgl3.> From 46 BC1plantsnts of RIL-46 M × 9930 (Table 1), two DNA pools, the M-pool (glabrous) and the WT-pool (non-glabrous), were constructed.
The two mutations were designated acdX1 and acdX2.
Expressed SEO genes containing frameshift mutations were designated as potential expressed pseudogenes.
Mutations were designated according to the Human Genome Variation Society guidelines (http://www.hgvs.org/mutnomen/).hgvs.org/mutnomen/
The clone containing 9 mutations was designated pS660.
The polarization of mutations was designated "ancestral nucleotide -to- current onucleotide -to- current
The presence of any one of the four PIK3CA mutations in a tumor was designated as PIK3CA mutation, whereas the absence of these four mutations was designated as PIK3CA wild-type.
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