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

Subjects

Subjects :

Genetics
SERPINC1 Gene
Deletion mutation
Hereditary Antithrombin Deficiency
Hematology
Multiplex ligation-dependent probe amplification
Biology
Molecular biology

Details

ISSN :

15387836

Volume :

6

Database :

OpenAIRE

Journal :

Journal of Thrombosis and Haemostasis

Accession number :

edsair.doi...........b1518501dce85da4eca32d971f217c75

Full Text :

https://doi.org/10.1111/j.1538-7836.2008.02905.x