Literature DB >> 18573519

Severe protein C deficiency from compound heterozygous mutations in the PROC gene in two Korean adult patients.

Hee-Jin Kim1, Duk-Kyung Kim, Kwang-Cheol Koh, Ji-Youn Kim, Sun-Hee Kim.   

Abstract

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Year:  2008        PMID： 18573519     DOI： 10.1016/j.thromres.2008.04.014

Source DB:  PubMed          Journal:  Thromb Res        ISSN： 0049-3848            Impact factor:   3.944


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  4 in total

1.  Three case reports of inherited antithrombin deficiency in China: double novel missense mutations, a nonsense mutation and a frameshift mutation.

Authors:  Haoyu Deng; Wei Shen; Yi Gu; Xiong Ma; Jiwei Zhang; Lan Zhang
Journal:  J Thromb Thrombolysis       Date:  2012-08       Impact factor: 2.300

2.  Impairment of protein C secretion in protein C-deficient patients carrying an Asp297 mutation.

Authors:  Jun Yamanouchi; Takaaki Hato; Toshiyuki Niiya; Tatsuya Hayashi; Koji Suzuki; Masaki Yasukawa
Journal:  Int J Hematol       Date:  2011-07-09       Impact factor: 2.490

3.  Distinct frequencies and mutation spectrums of genetic thrombophilia in Korea in comparison with other Asian countries both in patients with thromboembolism and in the general population.

Authors:  Hee-Jin Kim; Ja-Young Seo; Ki-O Lee; Sung-Hwan Bang; Seung-Tae Lee; Chang-Seok Ki; Jong-Won Kim; Chul Won Jung; Duk-Kyung Kim; Sun-Hee Kim
Journal:  Haematologica       Date:  2013-10-25       Impact factor: 9.941

4.  Hereditary thrombophilia in Korean patients with idiopathic pulmonary embolism.

Authors:  Mirae Lee; Hye Jin No; Shin Yi Jang; Nari Kim; Seung Hyuk Choi; Hojoong Kim; Sun-Hee Kim; Hee-Jin Kim; Duk-Kyung Kim
Journal:  Yonsei Med J       Date:  2012-05       Impact factor: 2.759
  4 in total

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