Budd-Chiari syndrome in a patient heterozygous for the point mutation C20221T of the prothrombin gene

Balim, ZKosova, BFalzon, KWettinger, SBColak, Y2019-10-272019-10-2720031538-7933https://doi.org/10.1046/j.1538-7836.2003.t01-2-00115.xhttps://hdl.handle.net/11454/36878en10.1046/j.1538-7836.2003.t01-2-00115.xinfo:eu-repo/semantics/closedAccessBudd-Chiari syndrome in a patient heterozygous for the point mutation C20221T of the prothrombin geneLetter14852853WOS:00018306210004012871427N/AQ4