S-EPMC10878193 - A single-center cohort study of patients with hereditary spherocytosis in Central Europe reveals a high frequency of novel disease-causing genotypes. - OmicsDI

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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.

ABSTRACT:

SUBMITTER: Kager L

PROVIDER: S-EPMC10878193 | biostudies-literature | 2024 Jan

REPOSITORIES: biostudies-literature