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TSC1 Mutations in Keratoconus Patients With or Without Tuberous Sclerosis
PURPOSE: To test candidate genes TSC1 and TSC2 in a family affected by tuberous sclerosis complex (TSC) where proband was also diagnosed with bilateral keratoconus (KC) and to test the hypothesis that defects in the same gene may lead to a nonsyndromic KC. METHODS: Next-generation sequencing of TSC1...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Association for Research in Vision and Ophthalmology
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760196/ https://www.ncbi.nlm.nih.gov/pubmed/29261847 http://dx.doi.org/10.1167/iovs.17-22819 |