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

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

216

Citations

28

References

1996

Year

Stefan Eber, Jennifer M. Reingle González, Marcia L. Lux, A L Scarpa, William Tse, Marion Dornwell, Jutta Herbers, Wilfried Kugler, Refik Özcan, Arnulf Pekrun,

Nature Genetics

Major CauseDevelopmental BiologyGenetic DisorderGeneticsMolecular GeneticsCytoskeletonAnkyrin–1 MutationsRecessive Hereditary SpherocytosisMedicineCell Biology

References

	Year	Citations

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