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A novel N491S mutation in the human SLC11A2 gene impairs ... | ResearchHub
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A novel N491S mutation in the human SLC11A2 gene impairs protein trafficking and in association with the G212V mutation leads to microcytic anemia and liver iron overload
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Authors
Edouard Bardou-Jacquet
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Edouard Bardou-Jacquet
•
Marie‐Laure Island
8 more
•
Olivier Loréal
Published
December 1, 2011
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Journal
Blood cells, molecules, & diseases/Blood cells, molecules & diseases
Topics
Biology
Biochemistry
Hematology
Mutation
Rna Splicing
Show all topics
DOI
10.1016/j.bcmd.2011.07.004