Antithrombin gene mutation 5356–5364delCTT with type I deficiency and early-onset thrombophilia and a brief review of the antithrombin α-helix D molecular pathology

Saved in:
Bibliographic Details
Published inAnnals of hematology Vol. 84; no. 7; pp. 485 - 486
Main Authors Steiner, M., Steiner, B., Rolfs, A., Wangnick, M., Burstein, C., Freund, M., Schuff-Werner, P.
Format Journal Article
LanguageEnglish
Published 01.07.2005
Online AccessGet full text

Cover

More Information
ISSN:0939-5555
1432-0584
DOI:10.1007/s00277-005-1045-1