Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome

被引：5

作者：

Minucci, Angelo ^{[1
]}

Ruggiero, Antonio ^{[2
]}

Canu, Giulia ^{[1
]}

Maurizi, Palma ^{[2
]}

De Bonis, Maria ^{[1
]}

Concolino, Paola ^{[1
]}

De Luca, Daniele ^{[1
,3
]}

Capoluongo, Ettore ^{[1
]}

机构：

[1] Lab Clin Mol & Personalized Diagnost, Dept Lab Med, Rome, Italy

[2] Univ Cattolica Sacro Cuore, Div Pediat Oncol, A Gemelli Hosp, Rome, Italy

[3] South Paris Univ Hosp, AP HP, A Beclere Med Ctr, Div Pediat & Neonatal Crit Care,FAME Dept, Paris, France

来源：

关键词：

PYRUVATE-KINASE DEFICIENCY; UDP-GLUCURONOSYLTRANSFERASE; HYPERBILIRUBINEMIA; GENE;

D O I：

10.1002/pbc.25500

中图分类号：

R73 [肿瘤学];

学科分类号：

100214 ;

摘要：

引用

页码：1680 / 1681

页数：2