Hofmann, Inga <br/><br/>
Congenital macrothrombocytopenia with focal myelofibrosis due to mutations in human G6b-B is rescued in humanized mice.  [electronic resource] 

 -  Blood  09 2018 
 - 1399-1412 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1528-0020 
<br/><br/><label>Standard No.: </label>10.1182/blood-2017-08-802769  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Animals<br/>Blood Platelets--metabolism<br/>Child<br/>Child, Preschool<br/>Female<br/>Gene Knock-In Techniques<br/>Humans<br/>Infant<br/>Loss of Function Mutation<br/>Male<br/>Megakaryocytes--metabolism<br/>Mice<br/>Mice, Inbred C57BL<br/>Mice, Knockout<br/>Pedigree<br/>Primary Myelofibrosis--congenital<br/>Receptors, Immunologic--genetics<br/>Thrombocytopenia--congenital<br/>Young Adult