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

dc.contributor.author

Patel, AJ

dc.contributor.author

Liu, H‐H

dc.contributor.author

Lager, RA

dc.contributor.author

Malkovska, V

dc.contributor.author

Zhang, B

dc.date.accessioned

2023-02-19T13:34:25Z

dc.date.available

2023-02-19T13:34:25Z

dc.date.issued

2013-07

dc.date.updated

2023-02-19T13:34:24Z

dc.identifier.issn

1351-8216

dc.identifier.uri

https://hdl.handle.net/10161/26636

dc.language

en

dc.publisher

Wiley

dc.relation.ispartof

Haemophilia

dc.relation.isversionof

10.1111/hae.12128

dc.title

Successful percutaneous coronary intervention in a patient with combined deficiency of FV and FVIII due to novel compound heterozygous mutations inLMAN1

dc.type

Journal article

pubs.begin-page

607

pubs.end-page

610

pubs.issue

4

pubs.organisational-group

Duke

pubs.organisational-group

Faculty

pubs.publication-status

Published

pubs.volume

19

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