Hereditary Spherocytosis in a Child due to a Deletion in β‐Spectrin Detected by Low‐Input DNA Long‐Read Whole‐Genome Sequencing
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Authors
- Vincent Schulz (ORCID: https://orcid.org/0000-0001-6333-4284)
- Melissa J. Rose (ORCID: https://orcid.org/0000-0003-0012-0734)
- Kiran Lalwani
- Patrick G. Gallagher (ORCID: https://orcid.org/0000-0002-5424-0224)
- Amanda Jacobson‐Kelly (ORCID: https://orcid.org/0000-0002-9118-4487)
- Liu Y (ORCID: https://orcid.org/0009-0004-3901-1652)
- Anthony R. Miller
- Richard K. Wilson
- Joyleen Oliver
Institutions
- Nationwide Children's Hospital (US)
- Yale University (US)
- The Ohio State University (US)
Publication Details
- Journal
- Pediatric Blood & Cancer
- Published
- 2026-07-23
- DOI
- https://doi.org/10.1002/1545-5017.70503
- Primary Topic
- Erythrocyte Function and Pathophysiology
- Type
- article
- Field-Weighted Citation Impact
- 0.00