RT Book, Section
A1 Tollefsen, Douglas M.
A2 Valle, David L.
A2 Antonarakis, Stylianos
A2 Ballabio, Andrea
A2 Beaudet, Arthur L.
A2 Mitchell, Grant A.
SR Print(0)
ID 1181455855
T1 Antithrombin Deficiency
T2 The Online Metabolic and Molecular Bases of Inherited Disease
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9780071459969
LK ommbid.mhmedical.com/content.aspx?aid=1181455855
RD 2024/04/19
AB This  update  summarizes  recent  advances  in  the  structure,  mechanism,  and  physiology  of  antithrombin  (gene  symbol  SERPINC1)  and  heparin  cofactor  II  (gene  symbol  SERPIND1,  alias  HCF2).  Current  recommendations  for  treatment  of  inherited  and  acquired  antithrombin  deficiency  are  reviewed  elsewhere.1  A  database  of  antithrombin  mutations  is  available  online  (http://www1.imperial.ac.uk/departmentofmedicine/divisions/experimentalmedicine/haematology/coag/antithrombin/).