Kuhle, S <br/><br/>
Homozygous antithrombin deficiency type II (99 Leu to Phe mutation) and childhood thromboembolism.  [electronic resource] 

 -  Thrombosis and haemostasis  Oct 2001 
 - 1007-11 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Review 
<br/><br/><label>ISSN: </label>0340-6245 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Age of Onset<br/>Amino Acid Substitution<br/>Antithrombin III--chemistry<br/>Antithrombin III Deficiency--epidemiology<br/>Binding Sites<br/>Brain Ischemia--genetics<br/>DNA Mutational Analysis<br/>Female<br/>Genetic Predisposition to Disease<br/>Genotype<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Infarction, Middle Cerebral Artery--genetics<br/>Male<br/>Mutation, Missense<br/>Point Mutation<br/>Thromboembolism--genetics<br/>Thrombophilia--epidemiology<br/>Venous Thrombosis--genetics<br/>Yugoslavia--epidemiology