Compound heterozygous mutations in the PROS1 gene responsible for quantitative and qualitative protein S deficiency

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Bibliographic Details
Published in	International journal of hematology Vol. 90; no. 4; pp. 537 - 539
Main Authors	Yamanouchi, Jun, Hato, Takaaki, Tamura, Tatsushiro, Fujiwara, Hiroshi, Yakushijin, Yoshihiro, Yasukawa, Masaki
Format	Journal Article
Language	English
Published	Tokyo Springer Japan 01.11.2009 Springer Springer Nature B.V
Subjects	Aged Biological and medical sciences Blood Proteins - genetics Hematologic and hematopoietic diseases Hematology Humans Letter to the Editor Male Medical sciences Medicine Medicine & Public Health Mutation Oncology Pedigree Platelet diseases and coagulopathies Protein S - genetics Protein S Deficiency - diagnosis Protein S Deficiency - genetics Venous Thrombosis - genetics PROS1 Mutation Human Embryo Kidney T617A Mutation Compound Heterozygous Mutation Nomenclature Working Group Hypercoagulability Thrombophilia Protein S deficiency Gene Hematology Genetics Hemopathy Mutation Coagulopathy Genetic disease Quantitative analysis Heterozygosity
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ISSN	0925-5710 1865-3774 1865-3774
DOI	10.1007/s12185-009-0430-2

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ISSN:	0925-5710 1865-3774 1865-3774
DOI:	10.1007/s12185-009-0430-2