Compound heterozygous protein C deficiency in a family with venous thrombosis: Identification and in vitro study of p.Asp297His and p.Val420Leu mutations-Reference-Cited by-同舟云学术

Compound heterozygous protein C deficiency in a family with venous thrombosis: Identification and in vitro study of p.Asp297His and p.Val420Leu mutations

Published:2015-05 Issue:1 Volume:563 Page:35-40
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Liu Hui,Wang Hua-Fang,Tang Liang,Yang Yan,Wang Qing-Yun,Zeng Wei,Wu Ying-Ying,Cheng Zhi-Peng,Hu Bei,Guo Tao,Hu Yu

Funder

National Natural Sciences Foundation of China

Natural Science Foundation of Hubei Province

Publisher

Elsevier BV

Subject

Genetics,General Medicine

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5. The phenotypic and genetic assessment of protein C deficiency;Cooper;Int. J. Lab. Hematol.,2012

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4. MiR-124 and miR-506 are involved in the decline of protein C in children with extra-hepatic portal vein obstruction;Scientific Reports;2021-06-10

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