Fullerton, S M <br/><br/>
Apolipoprotein E variation at the sequence haplotype level: implications for the origin and maintenance of a major human polymorphism.  [electronic resource] 

 -  American journal of human genetics  Oct 2000 
 - 881-900 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Standard No.: </label>10.1086/303070  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Alzheimer Disease--genetics<br/>Apolipoproteins E--genetics<br/>Base Sequence<br/>Cardiovascular Diseases--genetics<br/>Ethnicity--genetics<br/>Evolution, Molecular<br/>Finland<br/>Gene Frequency<br/>Genetic Variation--genetics<br/>Germ Cells--metabolism<br/>Haplotypes--genetics<br/>Heterozygote<br/>Humans<br/>Linkage Disequilibrium<br/>Mexico<br/>Missouri<br/>New York<br/>Nucleotides--genetics<br/>Polymorphism, Genetic--genetics<br/>Polymorphism, Single Nucleotide--genetics<br/>Protein Isoforms--genetics<br/>Regulatory Sequences, Nucleic Acid--genetics<br/>Time Factors