Mutational screening of VSX1 in keratoconus patients from the European population.

Dash, D P; George, S; O'Prey, D; Burns, D; Nabili, S; Donnelly, U; Hughes, A E; Silvestri, G; Jackson, J; Frazer, D; Héon, E; Willoughby, C E

Dash, D P; George, S; O'Prey, D; Burns, D; Nabili, S; Donnelly, U; Hughes, A E; Silvestri, G; Jackson, J; Frazer, D; Héon, E; Willoughby, C E.

Affiliation

Dash DP; Centre for Vision and Vascular Science, Queen's University Belfast, and Department of Ophthalmology, Royal Victoria Hospital, Belfast, Northern Ireland, UK.

Eye (Lond) ; 24(6): 1085-92, 2010 Jun.

Article in En | MEDLINE | ID: mdl-19763142

Subject(s)

Eye Proteins/genetics; Homeodomain Proteins/genetics; Keratoconus/genetics; Mutation; White People/genetics; DNA Mutational Analysis; Exons/genetics; Genetic Predisposition to Disease; Humans; Molecular Sequence Data; Sequence Analysis, DNA

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Homeodomain Proteins / White People / Eye Proteins / Keratoconus / Mutation Type of study: Diagnostic_studies / Screening_studies Limits: Humans Language: En Journal: Eye (Lond) Year: 2010 Document type: Article

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