Faiyaz-Ul-Haque, Muhammad <br/><br/>
A novel missense and a recurrent mutation in SLC2A10 gene of patients affected with arterial tortuosity syndrome.  [electronic resource] 

 -  Atherosclerosis  Apr 2009 
 - 466-71 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1879-1484 
<br/><br/><label>Standard No.: </label>10.1016/j.atherosclerosis.2008.07.026  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Arteries--pathology<br/>Connective Tissue Diseases--genetics<br/>Constriction, Pathologic<br/>DNA Mutational Analysis<br/>Family Health<br/>Female<br/>Glucose Transport Proteins, Facilitative--genetics<br/>Homozygote<br/>Humans<br/>Male<br/>Mutation<br/>Mutation, Missense<br/>Phenotype<br/>Saudi Arabia<br/>Syndrome