Barely Significant
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Mitochondrial mutations and polymorphisms in psychiatric disorders.

Front Genet · 2012 · PMC3379031 · PMID 22723804

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nominally significantno p-value reported
The logistic regression results were compared with the Ingman database of mtSNP frequencies to remove outlier nominally significant associations due to obvious miscalls with the Affymetrix genotyping platform.

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a positive trendno p-value reported
This is the first association study of mtDNA 16519T and 16519C variants in psychiatric disorders of BD, while a recent report showed a positive trend for SZ (Mosquera-Miguel et al., 2012 ).

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