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Successful percutaneous coronary intervention in a patient with combined deficiency of FV and FVIII due to novel compound heterozygous mutations in LMAN1

✍ Scribed by Patel, A. J.; Liu, H.-H.; Lager, R. A.; Malkovska, V.; Zhang, B.

Book ID: 120160265
Publisher: John Wiley and Sons
Year: 2013
Tongue: English
Weight: 162 KB
Volume: 19
Category: Article
ISSN: 1351-8216
DOI: 10.1111/hae.12128

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