Congenital factor XIII deficiency : A commentary on 'Homozygous intronic mutation leading to inefficient transcription combined with a novel frame-shift mutation in F13A1 gene causes FXIII deficiency'

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概要

• 論文の詳細を見る
• 2011-07-01

著者

• Shinozawa Keiko

  Department Of Laboratory Medicine Tokyo Medical University

関連論文

• Molecular Characterization of 3 Factor V mutations, R2174L, V1813M, and a 5-bp Deletion, That Cause Factor V Deficiency
• Mutations to the probe of Cobas TaqMan HIV-1 ver. 1.0 assay causing undetectable viral load in a patient with acute HIV-1 infection
• Congenital factor XIII deficiency : A commentary on 'Homozygous intronic mutation leading to inefficient transcription combined with a novel frame-shift mutation in F13A1 gene causes FXIII deficiency'

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