Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort-Impact of Selected Deep Intronic Variants and Common SNPs.

Invest Ophthalmol Vis Sci · 2017 · PMC5270621 · PMID 28118664

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closest p

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boldest claim

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highly significantno p-value reported

Still, STGD1 association of common variants c.1268A>G and c.5603A>T remained highly significant ( P values of 3.45E-05 and 4.82E-05, respectively).

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