✦ LIBER ✦
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
✍ Scribed by Minucci, Angelo; Canu, Giulia; Tellone, Ester; Giardina, Bruno; Zuppi, Cecilia; Capoluongo, Ettore
- Book ID
- 119194784
- Publisher
- Elsevier Science
- Year
- 2012
- Tongue
- English
- Weight
- 134 KB
- Volume
- 49
- Category
- Article
- ISSN
- 1079-9796
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