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

Identification of a polymorphism (D168N) in the XRP2 gene in Chinese.

Human mutation - 1 Apr 2001

Lin W D, Shi Y R, Tsai F J, Lee C C, Lin H J, Wu J Y

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to China
Share to Eye Proteins
Share to GTP-Binding Proteins
Share to Intracellular Signaling Peptides and Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Membrane Proteins

Share to Mutation, Missense

Share to Proteins

Share to Retinitis Pigmentosa

Source

Identifiers

PMID: 11295842
DOI: 10.1002/humu.43

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Identification of a polymorphism (D168N) in the XRP2 gene in Chinese.PMID 11295842Read ↗

Polymorphic study of XRCC1 G28152A and XRCC1 C26304T in 10 Chinese populations.Semantic proximity Read ↗

Two novel polymorphisms (c954T>C and c1038A>G) in exon8 of NPHS2 gene identified in Taiwan Chinese.Semantic proximity Read ↗

Classification of Missense Variants in XRCC2 by Functional Analysis: Implications for Breast Cancer Association Studies.Semantic proximity Read ↗

Haplotype analysis of XRCC2 gene polymorphisms and association with increased risk of head and neck cancer.Semantic proximity Read ↗

A RsaI polymorphism in the ERCC2 locus.Semantic proximity Read ↗

Genetic polymorphisms of DNA repair gene: XRCC1 Pro206Pro and Gln632Gln in a Chinese Han population.Semantic proximity Read ↗

A novel mutation with Ins C (882-883) of the factor X gene in a Taiwanese Chinese factor X-deficient family.Semantic proximity Read ↗

Novel c.435delC mutation in XK gene found in a Taiwanese patient with McLeod syndrome.Semantic proximity Read ↗

The Arg188His polymorphism in the XRCC2 gene and the risk of cancer.Semantic proximity Read ↗

Mutation characteristics of the PAH gene in four nationality groups in Xinjiang of China.Semantic proximity Read ↗

Localization, sequence analysis, and ethnic distribution of a 96-bp insertion in the promoter of the human CYP2E1 gene.Semantic proximity Read ↗

Factor XI deficiency as a result of a novel Tyr347Stop nonsense mutation in an elderly Japanese woman.Semantic proximity Read ↗

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