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

  • Angelo Minucci*
  • , Antonio Ruggiero
  • , Giulia Canu
  • , Palma Maurizi
  • , Maria De Bonis
  • , Paola Concolino
  • , Daniele De Luca
  • , Ettore Domenico Capoluongo
  • *Corresponding author
  • Department of Laboratory Medicine, Laboratory of Clinical Molecular and Personalized Diagnostics
  • Assistance publique – Hôpitaux de Paris

Research output: Contribution to journalArticle

Abstract

NO ABSTRACT AVALAIBLE
Original languageEnglish
Pages (from-to)1680-1681
Number of pages2
JournalPEDIATRIC BLOOD & CANCER
Volume62
Issue number9
DOIs
Publication statusPublished - 2015

All Science Journal Classification (ASJC) codes

  • Pediatrics, Perinatology, and Child Health
  • Hematology
  • Oncology

Keywords

  • PYRUVATE-KINASE DEFICIENCY
  • UDP-GLUCURONOSYLTRANSFERASE

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