No abstract

Minucci, A., Canu, G., Tellone, E., Giardina, B., Zuppi, C., Capoluongo, E. D., 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>>, 2012; 49 (2): 118-119. [doi:10.1016/j.bcmd.2012.05.004] [http://hdl.handle.net/10807/40067]

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;Giardina, Bruno;Zuppi, Cecilia;Capoluongo, Ettore Domenico
2012

Abstract

No abstract
Inglese
Minucci, A., Canu, G., Tellone, E., Giardina, B., Zuppi, C., Capoluongo, E. D., 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>>, 2012; 49 (2): 118-119. [doi:10.1016/j.bcmd.2012.05.004] [http://hdl.handle.net/10807/40067]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10807/40067
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