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

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2728569/
https://www.ncbi.nlm.nih.gov/pubmed/19693293

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