Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Study on relationship between Arg778Leu/Gln gene mutation spot in ATP7B and TCM syndrome type in Chinese patients with Wilson disease].

Zhongguo Zhong xi yi jie he za zhi Zhongguo Zhongxiyi jiehe zazhi = Chinese journal of integrated traditional and Western medicine - 1 Apr 2002

Yang Bin, Hu Ji-yuan, Hong Ming-fan

Abstract excerpt

OBJECTIVE: To investigate the relationship between Arg778Leu/Gln gene mutation spot in ATP7B and TCM Syndrome type in Chinese patients with Wilson disease (WD). METHODS: Exon 8 of ATP7B of 90 WD patients and 30 healthy controls were amplified by PCR and analysed by restriction enzyme Msp I, the TCM Syndrome type of the patients was differentiated at the same time. RESULTS: In the 90 WD patients, 34 with...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adenosine Triphosphatases
Share to Arginine

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cation Transport Proteins

Share to Copper-Transporting ATPases

Share to Diagnosis, Differential

Share to Hepatolenticular Degeneration

Share to Leucine

Share to Medicine, Chinese Traditional

Source

Identifiers

PMID: 12584791

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Study on relationship between Arg778Leu/Gln gene mutation spot in ATP7B and TCM syndrome type in Chinese patients with Wilson disease].PMID 12584791Read ↗

[Curative effect of TCM-WM therapy on Wilson disease with different clinical phenotypes and polymorphisms of ATP7B gene].Semantic proximity Read ↗

[Genotype-phenotype correlation of patients with wilson disease in Chinese population].Semantic proximity Read ↗

[Genotype and phenotype correlation in Chinese patients with Wilson's Disease].Semantic proximity Read ↗

[Identification of a novel missense mutation in Wilson disease gene].Semantic proximity Read ↗

[Study on mutation of exon 8 of Wilson's disease gene].Semantic proximity Read ↗

[Mutational analysis of ATP7B gene of hepatolenticular degeneration in Xinjiang region].Semantic proximity Read ↗

[Expression characters of ATP7B mRNA in liver tissue of patients with Wilson's disease].Semantic proximity Read ↗

Identification of a novel missense mutation in Wilson's disease gene.Semantic proximity Read ↗

[Using fluorescence PCR analysis for early diagnosis and carriers detection of Chinese Wilson's disease].Semantic proximity Read ↗

[Whole blood allele-specific PCR, a simple method to detect four ATP7B gene mutations in Wilson disease].Semantic proximity Read ↗

[A study of Wilson's disease gene encoded products and gene mutations].Semantic proximity Read ↗

[Effect of the mutation of promoter region in Wilson disease ATP7B gene on the expression of reporter gene].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.