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 Capoluongo; Ettore Domenico Capoluongo

doi:10.1002/pbc.25500

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 Capoluongo, Ettore Domenico Capoluongo

Department of Laboratory Medicine, Laboratory of Clinical Molecular and Personalized Diagnostics

Risultato della ricerca: Contributo in rivista › Articolo in rivista

2 Citazioni (Scopus)

Abstract

NO ABSTRACT AVALAIBLE

Lingua originale	English
pagine (da-a)	1680-1681
Numero di pagine	2
Rivista	PEDIATRIC BLOOD & CANCER
Volume	62
DOI	https://doi.org/10.1002/pbc.25500
Stato di pubblicazione	Pubblicato - 2015

Keywords

PYRUVATE-KINASE DEFICIENCY
UDP-GLUCURONOSYLTRANSFERASE

Accesso al documento

10.1002/pbc.25500

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

abstract = "NO ABSTRACT AVALAIBLE",

keywords = "PYRUVATE-KINASE DEFICIENCY, UDP-GLUCURONOSYLTRANSFERASE, PYRUVATE-KINASE DEFICIENCY, UDP-GLUCURONOSYLTRANSFERASE",

author = "Angelo Minucci and Antonio Ruggiero and Giulia Canu and Palma Maurizi and {De Bonis}, Maria and Paola Concolino and {De Luca}, Daniele and Ettore Capoluongo and Capoluongo, {Ettore Domenico}",

year = "2015",

doi = "10.1002/pbc.25500",

language = "English",

volume = "62",

pages = "1680--1681",

journal = "Pediatric Blood and Cancer",

issn = "1545-5009",

publisher = "Wiley Liss:111 River Street:Hoboken, NY 07030:(201)748-6000, (212)850-6645, EMAIL: subinfo@wiley.com, INTERNET: http://www.wiley.co.uk, Fax: (201)748-6088",

}

TY - JOUR

T1 - Co-inheritance of G6PD and PK deficiencies in a neonate carrying a Novel UGT1A1 genotype associated to Crigler-Najjar type II syndrome

AU - Minucci, Angelo

AU - Ruggiero, Antonio

AU - Canu, Giulia

AU - Maurizi, Palma

AU - De Bonis, Maria

AU - Concolino, Paola

AU - De Luca, Daniele

AU - Capoluongo, Ettore

AU - Capoluongo, Ettore Domenico

PY - 2015

Y1 - 2015

N2 - NO ABSTRACT AVALAIBLE

AB - NO ABSTRACT AVALAIBLE

KW - PYRUVATE-KINASE DEFICIENCY

KW - UDP-GLUCURONOSYLTRANSFERASE

KW - PYRUVATE-KINASE DEFICIENCY

KW - UDP-GLUCURONOSYLTRANSFERASE

UR - http://hdl.handle.net/10807/72374

U2 - 10.1002/pbc.25500

DO - 10.1002/pbc.25500

M3 - Article

SN - 1545-5009

VL - 62

SP - 1680

EP - 1681

JO - Pediatric Blood and Cancer

JF - Pediatric Blood and Cancer

ER -

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

Abstract

Keywords

Accesso al documento

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