Literature DB >> 18489710

Inherited protein S deficiency as a result of a large duplication mutation of the PROS1 gene detected by multiplex ligation-dependent probe amplification.

H-S Choung, H-J Kim, G-Y Gwak, S-H Kim, D-K Kim.   

Abstract

Entities:  

Mesh：

Substances：

Year:  2008        PMID： 18489710     DOI： 10.1111/j.1538-7836.2008.03026.x

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


× No keyword cloud information.
  3 in total

1.  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

2.  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

3.  Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency.

Authors:  Maria C Pintao; A A Garcia; D Borgel; M Alhenc-Gelas; C A Spek; M C H de Visser; S Gandrille; Pieter H Reitsma
Journal:  Hum Genet       Date:  2009-05-23       Impact factor: 4.132
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.