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Detection of large deletion mutations in the SERPINC1 gene causing hereditary antithrombin deficiency by multiplex ligation-dependent probe amplification (MLPA)

✍ Scribed by S.-T. LEE; H.-J. KIM; D.-K. KIM; R. J. L. SCHUIT; S.-H. KIM

Book ID: 109152463
Publisher: John Wiley and Sons
Year: 2008
Tongue: English
Weight: 139 KB
Volume: 6
Category: Article
ISSN: 1538-7933
DOI: 10.1111/j.1538-7836.2008.02905.x

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