Phenotype heterogeneity of hyperbilirubinemia condition:...

Blood Cells, Molecules, and Diseases 2012 / 8 Vol. 49; Iss. 2

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, Angelo, Canu, Giulia, Tellone, Ester, Giardina, Bruno, Zuppi, Cecilia, Capoluongo, Ettore
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Volume:
49
Language:
english
Journal:
Blood Cells, Molecules, and Diseases
DOI:
10.1016/j.bcmd.2012.05.004
Date:
August, 2012
File:
PDF, 134 KB
english, 2012
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