Magaña Torres, María Teresa <br/><br/>
Homozygous familial hypercholesterolemia: the c.1055G>A mutation in the LDLR gene and clinical heterogeneity.  [electronic resource] 

 -  Journal of clinical lipidology   
 - 525-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1933-2874 
<br/><br/><label>Standard No.: </label>10.1016/j.jacl.2014.05.002  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Child<br/>Child, Preschool<br/>Female<br/>Homozygote<br/>Humans<br/>Hyperlipoproteinemia Type II--drug therapy<br/>Male<br/>Middle Aged<br/>Mutation<br/>Pedigree<br/>Polymorphism, Genetic<br/>Receptors, LDL--genetics