Fournier, C M <br/><br/>
Spectrin St Claude, a splicing mutation of the human alpha-spectrin gene associated with severe poikilocytic anemia.  [electronic resource] 

 -  Blood  Jun 1997 
 - 4584-90 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0006-4971 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Alleles<br/>Anemia, Hemolytic, Congenital--blood<br/>Benin--ethnology<br/>Black People--genetics<br/>DNA, Complementary--genetics<br/>Erythrocytes, Abnormal<br/>Exons--genetics<br/>France<br/>Gene Frequency<br/>Genotype<br/>Guadeloupe--ethnology<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Mutagenesis, Insertional<br/>Mutation<br/>Open Reading Frames<br/>RNA Splicing<br/>RNA, Messenger--genetics<br/>Spectrin--genetics