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

✍ Scribed by Florian Gundel; Stefan Eber; Axel Heep

• Book ID: 105989633
• Publisher: Springer
• Year: 2010
• Tongue: English
• Weight: 59 KB
• Volume: 90
• Category: Article
• ISSN: 0939-5555
• DOI: 10.1007/s00277-010-0989-y