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

[A case of nt 1004C --> A G6PD gene mutation in Yunnan Han people].

Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi - 1 Oct 1997

Du C, He Y

Abstract excerpt

OBJECTIVE: To search for novel G6PD gene mutation in Yunnan. METHODS: After excluding common mutations among Chinese, 2 approximately 12 exons of G6PD gene were screened by PCR-SSCP, and those with an abnormal electrophoretic pattern were further sequenced. RESULTS: During a survey of G6PD deficiency in a population of 823 individuals in Yunnan, 54 cases were found with the deficiency. The gene mutations were...

Read the complete abstract on PubMed

Topics

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

Share to Asian People
Share to Base Sequence
Share to China

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Frequency

Share to Genotype

Share to Glucosephosphate Dehydrogenase

Share to Mutation

Source

Identifiers

PMID: 15625830

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[A case of nt 1004C --> A G6PD gene mutation in Yunnan Han people].PMID 15625830Read ↗

[Identification of G6PD gene mutations in several nationalities from Yunnan province].Semantic proximity Read ↗

[G6PD gene mutations in Guangxi, China].Semantic proximity Read ↗

[Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Han and Li nationalities in Hainan, China and identification of a new mutation in human G6PD gene].Semantic proximity Read ↗

[Molecular characterization of glucose-6-phosphate dehydrogenase variants in four ethnic groups in Yunnan province of China].Semantic proximity Read ↗

[Identification of three common G6PD gene mutations in Yi minority in Yunnan province].Semantic proximity Read ↗

[The genotype analysis of glucose-6-phosphate dehydrogenase deficiency in Yunnan province].Semantic proximity Read ↗

[Identification of mutations in the phenylalanine hydroxylase gene and exon 5 novel mutation Y166X(C-->G) in Yunnan].Semantic proximity Read ↗

[Common mutation analysis for patients found in Tianjin area with glucose-6-phosphate dehydrogenase deficiency].Semantic proximity Read ↗

[Genetic Mutation Characteristics of Glucose-6-Phosphate Dehydrogenase Deficiency Patients in Wuhan].Semantic proximity Read ↗

[Molecular epidemiology of G6PD deficiency in Chaozhou area of eastern Guangdong Province].Semantic proximity Read ↗

[Identification of G6PD mutations in Guangxi by combination of denaturing high performance liquid chromatography, DNA sequencing and restriction endonuclease analysis].Semantic proximity Read ↗

Incidence and complete molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Guangxi Zhuang autonomous region of southern China: description of four novel mutations.Semantic proximity Read ↗

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