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Molecular Diagnosis of Inherited Retinal Diseases in Indigenous African Populations by Whole-Exome Sequencing.

Invest Ophthalmol Vis Sci · 2016 · PMC5132076 · PMID 27898983

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almost insignificantno p-value reported
16 The most prevalent reported genetic defects in IRDs exhibit an almost insignificant incidence in the SA patient cohort. 17 – 20 Investigation of the indigenous African subcohort for reported mutations through the use of Asper Ophthalmics microarrays ( http://www.asperbio.com/asper-ophthalmics ; in the public domain) has produced lower returns in the indigenous African IRD subcohort than in the Caucasian subcohort.

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