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This subsequent mutation was a shock".
Presence of the GSTM1 mutation was determined through blood samples.
The T315I mutation was introduced by site-directed mutagenesis.
The absence of the FUS mutation was confirmed by sequencing.
JAK2V617F mutation was detected in 72% of all patients.
The ΔF508 mutation was found in 48.7% of the alleles.
And then we screened mutations, but no mutation was detected.
No mutation was found in any of the samples.
This mutation was named marR109.
The hemophilia mutation was just an accident.
An additional p16 mutation was identified.
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