Table 2.xls (5.5 kB)

Effect of CCL2 rs1024611 variants on disease phenotype.

Name: Effect of CCL2 rs1024611 variants on disease phenotype.
Published: 2018-04-17T17:25:06+00:00
License: https://creativecommons.org/licenses/by/4.0/
Keywords: CCR, AMD patients, univariate, ANCOVA, Allele frequency analysis, GG, AMD pathology, SNP, Total 171 subjects, Indian AMD Background, rs 1024611, genotype, rs 1024611 implicates prominence, CT, CCL -2 expression, CCL 2, rs 4586, TT, AG, MCP

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posted on 2018-04-17, 17:25 authored by Neel Kamal Sharma, Kaushal Sharma, Ramandeep Singh, Suresh Kumar Sharma, Akshay Anand

Effect of CCL2 rs1024611 variants on disease phenotype.

Effect of CCL2 rs1024611 variants on disease phenotype.

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