Familial segregation of a VSX1 mutation adds a new dimension to its role in the causation of keratoconus

PURPOSE: To look for segregation of Visual System Homeobox 1 (VSX1) mutations in family members of a patient with keratoconus. METHODS: Our initial molecular genetic studies conducted to identify the role of VSX1 in the causation of keratoconus had identified a novel mutation in one patient. He late...

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Detalles Bibliográficos
Autores principales: Paliwal, Preeti, Tandon, Radhika, Dube, Divya, Kaur, Punit, Sharma, Arundhati
Formato: Texto
Lenguaje:English
Publicado: Molecular Vision 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3042359/
https://www.ncbi.nlm.nih.gov/pubmed/21365019

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