Inherited protein S deficiency due to a novel nonsense mutation in the PROS1 gene in the patient with recurrent vascular access thrombosis: A case report

• Prif Awduron: Eun Jin Cho (Awdur), Yong Chul Kim (Awdur), Jin Ho Hwang (Awdur), Hajung Lee (Awdur), Sung Sup Park (Awdur), So Yeon Kim (Awdur), Suhnggwon Kim (Awdur), Ho Jun Chin (Awdur)
• Fformat: Llyfr
• Cyhoeddwyd: The Korean Society of Nephrology, 2012-03-01T00:00:00Z.
• Pynciau: article
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Vascular access thrombosis is one of the major causes of morbidity in patients maintained on chronic hemodialysis. Thrombophilia has been recognized as a risk factor of vascular access thrombosis. The authors report a case of inherited protein S deficiency associated with vascular access thrombotic...