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pro vyhledávání: '"Emmalee M. Kugler"'
Publikováno v:
Pediatric Hematology Oncology Journal, Vol 9, Iss 3, Pp 155-160 (2024)
Background: Heterozygous pathogenic variants of SPTB cause hereditary spherocytosis (HS) in a quarter of cases. Case report: A 14-day-old male presenting with persistent anemia and hyperbilirubinemia was diagnosed with HS by increased red blood cell
Externí odkaz:
https://doaj.org/article/d1b15cdef9424a61b2332bd3e7eb4722
