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

Publisher： John Wiley & Sons Inc

E-ISSN： 1545-5017|62|9|1680-1681

ISSN： 1545-5009

Source： PEDIATRIC BLOOD & CANCER (ELECTRONIC), Vol.62, Iss.9, 2015-09, pp. : 1680-1681

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