Case report: Genetic analysis of a novel intronic inversion variant in the SPTB gene associated with hereditary spherocytosis

Overview of attention for article published in Frontiers in Genetics, December 2023

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New Research: Case report: Genetic analysis of a novel intronic inversion variant in the SPTB gene associated with hereditary spherocytosis: Background: Hereditary spherocytosis (HS) is a congenital haemolytic anaemia attributed to… https://t.co/xjaZC99hzl

04 Dec 2023

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