Evaluation of the X-linked modifier loci for Leber hereditary optic neuropathy with the G11778A mutation in Chinese.

Mol Vis · 2010 · PMC2838738 · PMID 20300564

Europe PMC

hedged sentence

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closest p

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boldest claim

The sentences

highly significantno p-value reported

This marker is located in the broader linkage region but not in the highly significant fine mapping region reported by Hudson et al.

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