The genetics of Wilson disease. - Test2 - elhamkhani - TriplyDB

The genetics of Wilson disease.

The genetics of Wilson disease.

http://www.wikidata.org/entity/Q42380502

about

Dystonic Dysarthria in Wilson Disease: Efficacy of Zolpidem.

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Q45986951-F3AFAC1B-29A6-458D-9B2D-F7D678F07C5B

P2860

The genetics of Wilson disease.

http://www.wikidata.org/entity/Q42380502

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

name

The genetics of Wilson disease.

@en

The genetics of Wilson disease.

@nl

type

label

The genetics of Wilson disease.

@en

The genetics of Wilson disease.

@nl

prefLabel

The genetics of Wilson disease.

@en

The genetics of Wilson disease.

@nl

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B978-0-444-63625-6.00003-3

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Handbook of clinical neurology / edited by P.J. Vinken and G.W. Bruyn

P1476

The genetics of Wilson disease.

@en

P2093

Irene J Chang

http://www.w3.org/2001/XMLSchema#string

Si Houn Hahn

http://www.w3.org/2001/XMLSchema#string

P2860

Copper binding to the N-terminal metal-binding sites or the CPC motif is not essential for copper-induced trafficking of the human Wilson protein (ATP7B)

The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

Molecular mechanism of copper transport in Wilson disease.

Late onset fulminant Wilson's disease: a case report and review of the literature

Crystal structure of a copper-transporting PIB-type ATPase

Newborn screening: toward a uniform screening panel and system--executive summary

The nonsense-mediated decay RNA surveillance pathway

Elevated copper remodels hepatic RNA processing machinery in the mouse model of Wilson's disease

Genotype-phenotype correlations in a mountain population community with high prevalence of Wilson's disease: genetic and clinical homogeneity

Phenotype-genotype correlation in Wilson disease in a large Lebanese family: association of c.2299insC with hepatic and of p. Ala1003Thr with neurologic phenotype

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19-34

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scholarly article

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10.1016/B978-0-444-63625-6.00003-3

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142

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2017-01-01T00:00:00Z

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28433102

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5648646

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