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See Latest ArticlesA novel TACSTD2 mutation identified in two Chinese brothers with gelatinous drop-like corneal dystrophy
Molecular Vision, 08/19/09
Jing Y et al. – The newly identified mutation expands the spectrum of mutations in TACSTD2 that may cause pathological corneal amyloidosis. Observations by in vivo confocal microscopy and Fourier–domain OCT were consistent with the histopathologic descriptions of GDLD.
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