bibliographic resource 4683576 [br/4683576]
https://w3id.org/oc/corpus/br/4683576

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title
  • An isoform-specific mutation in the protein 4.1 gene results in hereditary elliptocytosis and complete deficiency of protein 4.1 in erythrocytes but not in nonerythroid cells.
publication date
  • 1993-01-01
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