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

被引：4
|
作者：
Minucci, Angelo [1 ]
Canu, Giulia [1 ]
Tellone, Ester [2 ]
Giardina, Bruno [1 ]
Zuppi, Cecilia [1 ]
Capoluongo, Ettore [1 ]
机构：
[1] Univ Cattolica Sacro Cuore, Dept Biochem & Clin Biochem, Lab Clin Mol Diagnost, Rome, Italy
[2] Univ Messina, Dept Biol Chem, I-98100 Messina, Italy
来源：
BLOOD CELLS MOLECULES AND DISEASES | 2012年 / 49卷 / 02期
关键词：
MUTATIONS; GENE;
D O I：
10.1016/j.bcmd.2012.05.004
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：118 / 119
页数：2
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