Brady, R O <br/><br/>
Enzymatic defect in Fabry's disease. Ceramidetrihexosidase deficiency.  [electronic resource] 

 -  The New England journal of medicine  May 1967 
 - 1163-7 p.  digital 
<br/><br/> Publication Type: Clinical Trial; Controlled Clinical Trial; Journal Article 
<br/><br/><label>ISSN: </label>0028-4793 
<br/><br/><label>Standard No.: </label>10.1056/NEJM196705252762101  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Angiokeratoma--genetics<br/>Biopsy<br/>Enzymes<br/>Female<br/>Glycolipids--metabolism<br/>Humans<br/>Intestinal Mucosa--enzymology<br/>Intestine, Small<br/>Lipid Metabolism, Inborn Errors<br/>Male<br/>Middle Aged<br/>Tritium