Young, S G <br/><br/>
Familial hypobetalipoproteinemia associated with a mutant species of apolipoprotein B (B-46).  [electronic resource] 

 -  The New England journal of medicine  Jun 1989 
 - 1604-10 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0028-4793 
<br/><br/><label>Standard No.: </label>10.1056/NEJM198906153202407  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Alleles<br/>Apolipoproteins B--blood<br/>Cholesterol, LDL--blood<br/>Female<br/>Heterozygote<br/>Humans<br/>Hypobetalipoproteinemias--genetics<br/>Hypolipoproteinemias--genetics<br/>Male<br/>Middle Aged<br/>Mutation<br/>Pedigree