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Recently, we have reported ABCC2 p.G693R mutation in 2 unrelated cases. In the present study, we investigated the pathogenicity of the ABCC2 p.G693R mutation in DJS in Asia. TECHNIQUES Clinical and hereditary evaluation was conducted when it comes to two customers aided by the ABCC2 p.G693R mutation. Whole exome sequencing for mutations in other understood hyperbilirubinemia-related genes was performed when it comes to situations w

https://glover-mcqueen-2.feder....atedjournals.com/thi
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