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Identification of mutations in the F9 gene including exon deletion by multiplex ligation-dependent probe amplification in 33 unrelated Korean patients with haemophilia B

โœ Scribed by M.-J. KWON; K.-Y. YOO; H.-J. KIM; S.-H. KIM


Book ID
108773103
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
259 KB
Volume
14
Category
Article
ISSN
1351-8216

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