Lanciotti, M <br/><br/>
Ankyrin deficiency is the most common defect in dominant and non dominant hereditary spherocytosis.  [electronic resource] 

 -  Haematologica   
 - 460-2 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0390-6078 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Ankyrins--deficiency<br/>Child<br/>Female<br/>Genes, Dominant<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Mutation<br/>Spherocytosis, Hereditary--genetics