Article

Exome sequencing for diagnosis of congenital hemolytic anemia

2020-05-19

Abstract excerpt

<title>Abstract</title> <p>Background: Congenital hemolytic anemia constitutes a heterogeneous group of rare genetic disorders of red blood cells. Diagnosis is based on clinical data, family history and phenotypic testing, genetic analyses being usually performed as a late step. In this study, we explored 40 patients with congenital hemolytic anemia by whole exome sequencing: 20 patients with hereditary spherocyt...

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Literature Corpus work: e8da2b7e-fe77-5afd-a201-341f0b34ee23
DOI: 10.21203/rs.2.24438/v2

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