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

Author： Sappal B.S.   Ghosh S.S.   Shneider B.   Kadakol A.   Chowdhury J.R.   Chowdhury N.R.  

Publisher： Elsevier

ISSN： 1096-7192

Source： Molecular Genetics and Metabolism, Vol.75, Iss.2, 2002-02, pp. : 134-142

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