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

Analysis of MC1R variants in Indian oculocutaneous albinism patients: highlighting the risk of skin cancer among albinos.

Journal of genetics - 1 Jan 2013

Sengupta Mainak, Sarkar Devroop, Mondal Maitreye, Samanta Swapan, Sil Asim, Ray Kunal

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 Albinism, Oculocutaneous
Share to Case-Control Studies
Share to DNA Mutational Analysis
Share to India

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Receptor, Melanocortin, Type 1

Share to Risk Factors

Share to Skin Neoplasms

Share to Young Adult

Source

Identifiers

PMID: 23970088
DOI: 10.1007/s12041-013-0250-2

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

Analysis of MC1R variants in Indian oculocutaneous albinism patients: highlighting the risk of skin cancer among albinos.PMID 23970088Read ↗

Melanocortin-1 receptor (MC1R): a review for dermatologists.Semantic proximity Read ↗

Behind the Scene: Exploiting MC1R in Skin Cancer Risk and Prevention.Semantic proximity Read ↗

A large French case-control study emphasizes the role of rare Mc1R variants in melanoma risk.Semantic proximity Read ↗

Spectrum of candidate gene mutations associated with Indian familial oculocutaneous and ocular albinism.Semantic proximity Read ↗

Two novel mutations detected in Japanese patients with oculocutaneous albinism.Semantic proximity Read ↗

MC1R mutations modify the classic phenotype of oculocutaneous albinism type 2 (OCA2).Semantic proximity Read ↗

Albinism research in a Southern African setting: unique findingsSemantic proximity Read ↗

Comprehensive evaluation of allele frequency differences of MC1R variants across populations.Semantic proximity Read ↗

Impact of homozygosity of R151C variant of MC1r in human hair follicle melanocytes.Semantic proximity Read ↗

Genetic analyses of oculocutaneous albinism types 1 and 2 with four novel mutationsSemantic proximity Read ↗

MC1R gene variants and non-melanoma skin cancer: a pooled-analysis from the M-SKIP project.Semantic proximity Read ↗

Influence of loss of function MC1R variants in genetic susceptibility of familial melanoma in Spain.Semantic proximity Read ↗

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