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In this paper, we discuss other aspects of the disease, including laboratory examination, homogeneous sequence alignment and molecular modeling. We reported a novel homozygous mutation in the F13A1 gene in a factor XIII (FXIII)-deficient patient, which adds a new point mutation to the mutant library. In this paper, we discuss other aspects of the disease, including laboratory examination, homogeneous sequence alignment and molecular modeling. In 1997, the Radiation Therapy Oncology Group (RTOG) put forward the recursive partitioning a
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