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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...
Autores principales: | Jing, Yang, Liu, Chun, Wang, Liya |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Molecular Vision
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2728569/ https://www.ncbi.nlm.nih.gov/pubmed/19693293 |
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