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A novel TACSTD2 mutation identified in two Chinese brothers with gelatinous drop-like corneal dystrophy

PURPOSE: To identify the molecular defect causing gelatinous drop-like corneal dystrophy (GDLD) in two Chinese brothers and report the morphological evaluation of GDLD by laser scanning confocal microscopy and Fourier-domain optical coherence tomography (OCT). METHODS: Genetic analysis included poly...

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Bibliografische gegevens
Hoofdauteurs: Jing, Yang, Liu, Chun, Wang, Liya
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Molecular Vision 2009
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2728569/
https://ncbi.nlm.nih.gov/pubmed/19693293
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