UGT1A1 Genotype in a white boy with Crigler-Najjar syndrome type 2

ROSATELLI, MARIA CRISTINA;
2012-01-01
2012
Bilirubin; Glucuronosyltransferase 1A1; Crigler Najjar syndrome; Crigler Najjar syndrome type 2; Gene; Gene frequency; Gene mutation; Genotype; Homozygote; Human; Hyperbilirubinemia
Files in This Item:
File Size Format  
_A rare UGT1A1 genotype causes Crigler-Najjar syndrome type 2 in a Caucasian boy.pdf

Solo gestori archivio

Type: versione editoriale
Size 56.29 kB
Format Adobe PDF
& nbsp; View / Open   Request a copy
56.29 kB Adobe PDF & nbsp; View / Open   Request a copy

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Questionnaire and social

Share on:
Impostazioni cookie