Mañú-Pereira, María Del Mar <br/><br/>
Pyruvate kinase deficiency and severe congenital hemolytic anemia in a double heterozygous patient with paternal transmission of an early germ-line de novo mutation.  [electronic resource] 

 -  American journal of hematology  Dec 2015 
 - E217-9 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1096-8652 
<br/><br/><label>Standard No.: </label>10.1002/ajh.24178  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Anemia, Hemolytic, Congenital--genetics<br/>Anemia, Hemolytic, Congenital Nonspherocytic--genetics<br/>Germ-Line Mutation<br/>Humans<br/>Male<br/>Paternal Exposure<br/>Pyruvate Kinase--deficiency<br/>Pyruvate Metabolism, Inborn Errors--genetics