Lab co-authors 5th report of TBK1 mutations in glaucoma patients.

Mon, 11/24/2014 - 08:45
We report discovery of TBK1 gene defects (abnormalities in the number of TBK1 genes in the genome) in another cohort of patients, the patients studied by the NEIGHBORHOOD study group. The manuscript is now available at in the Papers In Press section.
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Fingert Lab