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A new ankyrin mutation (ANK1 EXON E9X) causing severe hereditary spherocytosis in the neonatal period.

AuthorsFlorian Gundel, Stefan Eber, Axel Heep
JournalAnnals of hematology (Ann Hematol) Vol. 90 Issue 2 Pg. 231-2 (Feb 2011) ISSN: 1432-0584 [Electronic] Germany
PMID20512576 (Publication Type: Case Reports, Letter)
Chemical References
  • Ankyrins
Topics
  • Ankyrins (genetics)
  • Exons
  • Humans
  • Infant, Newborn
  • Infant, Newborn, Diseases (genetics)
  • Male
  • Mutation
  • Spherocytosis, Hereditary (genetics)

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