Article

Clinical manifestations and phenotypic analysis of new ANK1 gene mutations in 12 Chinese children with hereditary spherocytosis

2019-05-15

Abstract excerpt

<h4>Objective</h4> To summarize the clinical features and laboratory examination of ANK1 gene in 12 children with hereditary spherocytosis in China, and to determine the genetic mutations in those children. <h4>Methods</h4> The clinical data of children and their parents were collected and analyzed. The sequence of related genes was analyzed by second-generation sequencing technology. The suspected pathogenic mu...

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Literature Corpus work: 6b84111d-3afd-54da-be10-8c61acb8fa9c
DOI: 10.1101/637553

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