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Article

A novel deletion mutation of ATP7A gene in a Chinese family with Menkes disease.

Chinese medical journal - 20 Jan 2008

Zhang Li-ping, Lü Jun-lan, Wang Xiao-hui, Zou Li-ping

Abstract excerpt

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Share to Adenosine Triphosphatases
Share to Cation Transport Proteins
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 18272047
DOI: 10.3901/jme.2008.05.175

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A novel deletion mutation of ATP7A gene in a Chinese family with Menkes disease.PMID 18272047Read ↗

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Identification of a novel mutation in the ATP7A gene in a Korean patient with Menkes disease.Semantic proximity Read ↗

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Phenotypic and mutational spectrum of 17 Chinese patients with Menkes Disease.Semantic proximity Read ↗

Two novel mutations of the ATP2C1 gene in Chinese families with Hailey-Hailey disease.Semantic proximity Read ↗

[Clinical and genetic analysis of three children with Menkes disease due to variants of ATP7A gene].Semantic proximity Read ↗

[Analysis of clinical characteristics and ATP7A gene variants in a Chinese pedigree affected with Menkes disease].Semantic proximity Read ↗

Identification of novel ATP7A mutations and prenatal diagnosis in Chinese patients with Menkes disease.Semantic proximity Read ↗

Two novel mutations in the ATP2A2 gene in Chinese patients with Darier disease.Semantic proximity Read ↗

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