Article
Phenotype heterogeneity of hyperbilirubinemia condition: the lesson by coinheritance of glucose-6-phosphate dehydrogenase deficiency and Crigler-Najjar syndrome type II in an Italian patient.
Blood cells, molecules & diseases - 15 Aug 2012
Minucci Angelo, Canu Giulia, Tellone Ester, Giardina Bruno, Zuppi Cecilia, Capoluongo Ettore
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