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.

No abstract is available for this paper.

• Publication year

  2012

• Venue

  Blood Cells, Molecules & Diseases

• Publication date

  2012-08-15

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1016/j.bcmd.2012.05.004PMID 22633750
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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