Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic analysis.
about
Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic analysis.
description
2014 nî lūn-bûn
@nan
2014 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Crigler-Najjar syndrome type I ...... and a family genetic analysis.
@ast
Crigler-Najjar syndrome type I ...... and a family genetic analysis.
@en
Crigler-Najjar syndrome type I ...... sphate-glucuronosyltransferase
@nl
type
label
Crigler-Najjar syndrome type I ...... and a family genetic analysis.
@ast
Crigler-Najjar syndrome type I ...... and a family genetic analysis.
@en
Crigler-Najjar syndrome type I ...... sphate-glucuronosyltransferase
@nl
prefLabel
Crigler-Najjar syndrome type I ...... and a family genetic analysis.
@ast
Crigler-Najjar syndrome type I ...... and a family genetic analysis.
@en
Crigler-Najjar syndrome type I ...... sphate-glucuronosyltransferase
@nl
P2093
P2860
P356
P1433
P1476
Crigler-Najjar syndrome type I ...... and a family genetic analysis.
@en
P2093
P2860
P2888
P356
10.1186/1471-2431-14-267
P577
2014-10-15T00:00:00Z
P5875
P6179
1012545352