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Co‐inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler–Najjar type II syndrome
Author(s) -
Minucci Angelo,
Ruggiero Antonio,
Canu Giulia,
Maurizi Palma,
De Bonis Maria,
Concolino Paola,
De Luca Daniele,
Capoluongo Ettore
Publication year - 2015
Publication title -
pediatric blood and cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.116
H-Index - 105
eISSN - 1545-5017
pISSN - 1545-5009
DOI - 10.1002/pbc.25500
Subject(s) - medicine , personalized medicine , pediatrics , family medicine , bioinformatics , biology
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