Identification of one novel and nine recurrent mutations of the ATP7B gene in 11 children with Wilson disease.
about
Characterization of timed changes in hepatic copper concentrations, methionine metabolism, gene expression, and global DNA methylation in the Jackson toxic milk mouse model of Wilson disease.Novel mutations of the ATP7B gene in Han Chinese families with pre-symptomatic Wilson's disease.Identification and characterization of a novel 43-bp deletion mutation of the ATP7B gene in a Chinese patient with Wilson's disease: a case report.
P2860
Identification of one novel and nine recurrent mutations of the ATP7B gene in 11 children with Wilson disease.
description
2012 nî lūn-bûn
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2012年の論文
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2012年学术文章
@wuu
2012年学术文章
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2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh-hant
name
Identification of one novel an ...... children with Wilson disease.
@en
Identification of one novel an ...... children with Wilson disease.
@nl
type
label
Identification of one novel an ...... children with Wilson disease.
@en
Identification of one novel an ...... children with Wilson disease.
@nl
prefLabel
Identification of one novel an ...... children with Wilson disease.
@en
Identification of one novel an ...... children with Wilson disease.
@nl
P2093
P2860
P1476
Identification of one novel an ...... children with Wilson disease.
@en
P2093
Xiao-Qing Liu
P2860
P2888
P304
P356
10.1007/S12519-012-0388-7
P577
2012-12-29T00:00:00Z