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A Novel Intronic Mutation Results in the Use of a Cryptic Splice Acceptor Site within the Coding Region of UGT1A1, Causing Crigler-Najjar Syndrome Type 1

✍ Scribed by Baljit S. Sappal; Siddhartha S. Ghosh; Benjamin Shneider; Ajit Kadakol; Jayanta Roy Chowdhury; Namita Roy Chowdhury

No coin nor oath required. For personal study only.

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