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 / Minucci, A; Canu, G; Tellone, E; Giardina, B; Zuppi, C; Capoluongo, E. - In: BLOOD CELLS, MOLECULES, & DISEASES. - ISSN 1079-9796. - 49:2(2012), pp. 118-119. [10.1016/j.bcmd.2012.05.004]
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
Capoluongo E
2012
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