A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis-Reference-Cited by-同舟云学术

A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis

Published:2011-03 Issue:3 Volume:39 Page:305-320.e2
ISSN:0301-472X
Container-title:Experimental Hematology
language:en
Short-container-title:Experimental Hematology

Author:

Hughes Michael R.,Anderson Nicole,Maltby Steven,Wong Justin,Berberovic Zorana,Birkenmeier Connie S.,Haddon D. James,Garcha Kamal,Flenniken Ann,Osborne Lucy R.,Adamson S. Lee,Rossant Janet,Peters Luanne L.,Minden Mark D.,Paulson Robert F.,Wang Chen,Barber Dwayne L.,McNagny Kelly M.,Stanford William L.

Publisher

Elsevier BV

Subject

Cancer Research,Cell Biology,Genetics,Hematology,Molecular Biology

Reference37 articles.

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3. Clinical utility of targeted gene enrichment and sequencing technique in the diagnosis of adult hereditary spherocytosis;Annals of Translational Medicine;2019-10

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