Article

Mutation spectrum and biochemical features in infants with neonatal Dubin-Johnson syndrome

2020-07-31

Abstract excerpt

<title>Abstract</title> <p><bold>Background:</bold> Dubin-Johnson syndrome (DJS) is an autosomal recessive disorder presenting as isolated direct hyperbilirubinemia.DJS is rarely diagnosed in the neonatal period. The purpose of this study was to clarify the clinical features of neonatal DJS and to analyze the genetic mutation of adenosine triphosphate-binding cassette subfamily C member 2 (<italic>ABCC2</italic>)...

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Literature Corpus work: 8b991df1-85c3-5555-98e5-58776281df6b
DOI: 10.21203/rs.2.21832/v3

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