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Article

Hemolytic anemia in the mouse. Report of a new mutation and clarification of its genetics.

The Journal of heredity - 1 Jan 2000

Unger A E, Harris M J, Bernstein S E, Falcone J C, Lux S E

Abstract excerpt

A new mutation causing spherocytic, hemolytic anemia has been discovered in the house mouse. It is inherited as a single autosomal recessive gene, allelic with both sph and ha, which, in turn, were shown to be allelic with each other. A revised nomenclature for the three apparent alleles is proposed: sph (formerly sph), sphha (formerly ha), and sph2Bc (the new mutation). Like the other murine hemolytic anemias,...

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Identifiers

PMID: 6841965
DOI: 10.1093/oxfordjournals.jhered.a109747

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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