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Article

Lack of association of CCR2-64I and CCR5-Delta 32 with type 1 diabetes and latent autoimmune diabetes in adults.

Human immunology - 1 Jun 2003

Gambelunghe Giovanni, Ghaderi Mehran, Brozzetti Annalisa, Del Sindaco Paola, Gharizadeh Babeck, Nyren Paul, Hjelmström Peter, Nikitina-Zake Liene, Sanjeevi Carani B, Falorni Alberto

Abstract excerpt

It is well known that type 1 diabetes mellitus (T1DM) is a complex genetic disease resulting from the autoimmune destruction of pancreatic beta cells. Several genes have been associated with susceptibility and/or protection for T1DM, but the disease risk is mostly influenced by genes located in the class II region of the major histocompatibility complex. The attraction of leukocytes to tissues is essential for...

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Share to Amino Acid Substitution
Share to Diabetes Mellitus, Type 1

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Point Mutation

Share to Receptors, CCR2

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Share to Sequence Deletion

Source

Identifiers

PMID: 12770795
DOI: 10.1016/s0198-8859(03)00064-8

Genes

CCR2
CCR5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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