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Confirmation and Refinement of the Heterozygous Deletion of the Small Leucine-rich Proteoglycans Associated with Posterior Amorphous Corneal Dystrophy
PURPOSE: To present the clinical and cytogenetic features of a previously unreported family with posterior amorphous corneal dystrophy (PACD) associated with a heterozygous deletion of the small leucine-rich proteoglycan genes on chromosome 12. METHODS: Clinical characterization was performed using...
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| Publicado no: | Ophthalmic Genet |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6309915/ https://ncbi.nlm.nih.gov/pubmed/29671669 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/13816810.2018.1459736 |
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