Weidle, E G <br/><br/>
[Corneal opacity as the leading symptom of hereditary lecithin-cholesterol acyltransferase (LCAT) deficiency. Case report and a review of the literature].  [electronic resource] 

 -  Klinische Monatsblatter fur Augenheilkunde  Mar 1987 
 - 182-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0023-2165 
<br/><br/><label>Standard No.: </label>10.1055/s-2008-1050353  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Corneal Opacity--genetics<br/>Corneal Stroma--pathology<br/>Female<br/>Humans<br/>Hypolipoproteinemias--genetics<br/>Lecithin Cholesterol Acyltransferase Deficiency--genetics<br/>Pedigree