Genetic analysis of 55 northern Vietnamese patients with Wilson disease: seven novel mutations in ATP7B.

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Genetic analysis of 55 northern Vietnamese patients with Wilson disease: seven novel mutations in ATP7B.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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2017年學術文章

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Genetic analysis of 55 norther ...... even novel mutations in ATP7B.

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Genetic analysis of 55 norther ...... even novel mutations in ATP7B.

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Genetic analysis of 55 norther ...... even novel mutations in ATP7B.

@en

Genetic analysis of 55 norther ...... even novel mutations in ATP7B.

@nl

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Genetic analysis of 55 norther ...... even novel mutations in ATP7B.

@en

Genetic analysis of 55 norther ...... even novel mutations in ATP7B.

@nl

P1476

Genetic analysis of 55 norther ...... even novel mutations in ATP7B.

@en

P2093

Cam Tu Ho

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Dat Quoc Tran

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Hoang Bich Nga Le

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Le Anh Tuan Pham

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The Hung Bui

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Thinh Huy Tran

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Trong Tue Nguyen

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Van Khanh Tran

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Van Thanh Ta

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P2860

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

Persistent hypertransaminasemia in asymptomatic children: a stepwise approach

The Menkes/Wilson disease gene homologue in yeast provides copper to a ceruloplasmin-like oxidase required for iron uptake.

The Wilson's disease gene and phenotypic diversity.

The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene.

ATP7B (WND) protein.

His1069Gln and six novel Wilson disease mutations: analysis of relevance for early diagnosis and phenotype.

Correlation of ATP7B genotype with phenotype in Chinese patients with Wilson disease.

A genetic study of Wilson's disease in the United Kingdom

High frequency of the c.3207C>A (p.H1069Q) mutation in ATP7B gene of Lithuanian patients with hepatic presentation of Wilson's disease.

P2888

s12041-017-0857-9

P304

933-939

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P31

scholarly article

P356

10.1007/S12041-017-0857-9

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P433

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P478

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P577

2017-12-01T00:00:00Z

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P698

29321352

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