Genetic variance in the spinocerebellar ataxia type 2 (ATXN2) gene in children with severe early onset obesity.

PLoS One · 2009 · PMC2791421 · PMID 20016785

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nominally significantno p-value reported

Nonsense mutations, or changes near exon-intron boundaries were absent in the 92 samples, One synonymous coding SNP (rs695872), and one intronic SNP (rs2073950) showed nominally significant deviations from genotype frequencies reported for the CEU population sample.

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