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Case Reports
. 2015 Sep;62(9):1680-1.
doi: 10.1002/pbc.25500. Epub 2015 Mar 27.

Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome

Angelo Minucci  1 , Antonio Ruggiero  2 , Giulia Canu  1 , Palma Maurizi  2 , Maria De Bonis  1 , Paola Concolino  1 , Daniele De Luca  1   3 , Ettore Capoluongo  1
Affiliations
Case Reports

Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome

Angelo Minucci et al. Pediatr Blood Cancer. 2015 Sep.
No abstract available

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