Rost, Simone <br/><br/>
Founder mutation Arg485Pro led to recurrent compound heterozygous GGCX genotypes in two German patients with VKCFD type 1.  [electronic resource] 

 -  Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis  Sep 2006 
 - 503-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0957-5235 
<br/><br/><label>Standard No.: </label>10.1097/01.mbc.0000240927.88177.d1  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Carbon-Carbon Ligases--genetics<br/>Conserved Sequence--genetics<br/>Female<br/>Founder Effect<br/>Haplotypes--genetics<br/>Humans<br/>Infant<br/>Male<br/>Mixed Function Oxygenases--deficiency<br/>Sequence Analysis, DNA<br/>Vitamin K--administration & dosage<br/>Vitamin K Epoxide Reductases