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Characteristics of patients with and without major arrhythmia recurrence are described in the Table 1.
The difference in stand volume between the treatments, using the second treatment as the base, the significance of the comparison and context are described in the table.
Primer sequences and cycling conditions are described in the Table S1.
Genotyping was performed by PCR using genomic DNA extracted from tail clips (lysis with of 100 mM NaCl, 10 mM Tris pH 8.0, 25 mM EDTA pH 8.0, 0.5% SDS, and 2.5 ug/ml Proteinase K followed by phenol-chloroform extraction and ethanol precipitation) or Sigma REDExtract-N-Amp™ Tissue PCR kit (primers are described in the Table S1).
These are described in the Table 1.
The source databases are described in the table 1.
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Further particulars of patients are described in the tables.
The product is described in the (Table 2).
The demographic and clinical information for the patients is described in the Table.
The treatment regimen and duration for each patient is described in the table.
The detailed surface histomorphological change of each specimen was described in the Table 1.
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