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Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis.

Details

Language :
English
ISSN :
10614036
Volume :
13
Issue :
2
Database :
Complementary Index
Journal :
Nature Genetics
Publication Type :
Academic Journal
Accession number :
60965945
Full Text :
https://doi.org/10.1038/ng0696-214