Literature DB >> 18208532

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

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

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Year:  2008        PMID： 18208532     DOI： 10.1111/j.1538-7836.2008.02905.x

Source DB:  PubMed          Journal:  J Thromb Haemost        ISSN： 1538-7836            Impact factor:   5.824


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  3 in total

1.  High prevalence of congenital thrombophilia in patients with pregnancy-related or idiopathic venous thromboembolism/pulmonary embolism.

Authors:  Makoto Ikejiri; Hideo Wada; Norikazu Yamada; Maki Nakamura; Naoki Fujimoto; Kaname Nakatani; Akimasa Matsuda; Yosihito Ogihara; Takeshi Matsumoto; Yuki Kamimoto; Tomoaki Ikeda; Naoyuki Katayama; Masaaki Ito
Journal:  Int J Hematol       Date:  2016-10-20       Impact factor: 2.490

2.  Heterogeneous lengths of copy number mutations in human coagulopathy revealed by genome-wide high-density SNP array.

Authors:  Hee-Jin Kim; Duk-Kyung Kim; Ki-Young Yoo; Chur-Woo You; Jong-Ha Yoo; Ki-O Lee; In-Ae Park; Hae-Sun Choung; Hee-Jung Kim; Min-Jung Song; Sun-Hee Kim
Journal:  Haematologica       Date:  2011-10-11       Impact factor: 9.941

3.  Detection and characterisation of large SERPINC1 deletions in type I inherited antithrombin deficiency.

Authors:  Véronique Picard; Jian-Min Chen; Brigitte Tardy; Marie-Françoise Aillaud; Christine Boiteux-Vergnes; Marie Dreyfus; Joseph Emmerich; Cécile Lavenu-Bombled; Ulrike Nowak-Göttl; Nathalie Trillot; Martine Aiach; Martine Alhenc-Gelas
Journal:  Hum Genet       Date:  2009-09-17       Impact factor: 4.132
  3 in total

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