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.
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| Description | scientific article |
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author: Giulia Canu Bruno Giardina Angelo Minucci Cecilia Zuppi Ettore Capoluongo |
| Publication date | May 25, 2012 |
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