Miraglia del Giudice, E <br/><br/>
Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiency.  [electronic resource] 

 -  British journal of haematology  May 1998 
 - 251-4 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0007-1048 
<br/><br/><label>Standard No.: </label>10.1046/j.1365-2141.1998.00688.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Child, Preschool<br/>Female<br/>Gene Expression<br/>Heterozygote<br/>Humans<br/>Infant<br/>Male<br/>Mutation<br/>Pedigree<br/>Polymorphism, Genetic<br/>RNA, Messenger--metabolism<br/>Spectrin--deficiency<br/>Spherocytosis, Hereditary--genetics