Detection of large deletion mutations in the SERPINC1 gene causing hereditary antithrombin deficiency by multiplex ligation-dependent probe amplification (MLPA) [1]

S. T. Lee; Hee Jin Kim; D. K. Kim; R. J.L. Schuit; S. H. Kim

doi:10.1111/j.1538-7836.2008.02905.x

Detection of large deletion mutations in the SERPINC1 gene causing hereditary antithrombin deficiency by multiplex ligation-dependent probe amplification (MLPA) [1]

S. T. Lee
, Hee Jin Kim
, D. K. Kim
, R. J.L. Schuit
, S. H. Kim

Department of Laboratory Medicine and Genetics

Sungkyunkwan University
MRC-Holland

Research output: Contribution to journal › Letter › peer-review

17 Scopus citations

Original language	English
Pages (from-to)	701-703
Number of pages	3
Journal	Journal of Thrombosis and Haemostasis
Volume	6
Issue number	4
DOIs	https://doi.org/10.1111/j.1538-7836.2008.02905.x
State	Published - Apr 2008

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10.1111/j.1538-7836.2008.02905.x

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title = "Detection of large deletion mutations in the SERPINC1 gene causing hereditary antithrombin deficiency by multiplex ligation-dependent probe amplification (MLPA) [1]",

author = "Lee, \{S. T.\} and Kim, \{Hee Jin\} and Kim, \{D. K.\} and Schuit, \{R. J.L.\} and Kim, \{S. H.\}",

year = "2008",

month = apr,

doi = "10.1111/j.1538-7836.2008.02905.x",

language = "English",

volume = "6",

pages = "701--703",

journal = "Journal of Thrombosis and Haemostasis",

issn = "1538-7933",

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T1 - Detection of large deletion mutations in the SERPINC1 gene causing hereditary antithrombin deficiency by multiplex ligation-dependent probe amplification (MLPA) [1]

AU - Lee, S. T.

AU - Kim, Hee Jin

AU - Kim, D. K.

AU - Schuit, R. J.L.

AU - Kim, S. H.

PY - 2008/4

Y1 - 2008/4

UR - https://www.scopus.com/pages/publications/40949086763

U2 - 10.1111/j.1538-7836.2008.02905.x

DO - 10.1111/j.1538-7836.2008.02905.x

M3 - Letter

C2 - 18208532

AN - SCOPUS:40949086763

SN - 1538-7933

VL - 6

SP - 701

EP - 703

JO - Journal of Thrombosis and Haemostasis

JF - Journal of Thrombosis and Haemostasis

IS - 4

ER -

Detection of large deletion mutations in the SERPINC1 gene causing hereditary antithrombin deficiency by multiplex ligation-dependent probe amplification (MLPA) [1]

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