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A single-center cohort study of patients with hereditary spherocytosis in Central Europe reveals a high frequency of novel disease-causing genotypes.

Document Type

Article

Author

Kager, Leo; Jimenez-Heredia, Raúl; Zeitlhofer, Petra; Novak, Wolfgang; Eder, Sebastian K.; Segarra-Roca, Anna; Frohne, Alexandra; Nebral, Karin; Haimel, Matthias; Geyeregger, René; Roetzer-Londgin, Katharina; Haas, Oskar A.; Boztug, Kaan

Source

HemaSphere; Jan2024, Vol. 8 Issue 1, p1-6, 6p

Subject

Language

ISSN

25729241

Online Access

Full Text (LWW Journals - Ovid) Full Text (LWW total - Ovid) Full Text (ProQuest Central) Open Access (Wiley) Web of Science Scopus Find it@PNU

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