Recurrent pulmonary embolism in a 13-year-old male homozygous for the prothrombin G20210A mutation combined with protein S deficiency and increased lipoprotein (a)

Author: Kosch A.   Junker R.   Wermes C.   Nowak-Gottl U.  

Publisher: Elsevier

ISSN: 0049-3848

Source: Thrombosis Research, Vol.105, Iss.1, 2002-01, pp. : 49-53

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content