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SLC4A11 mutations in Fuchs endothelial corneal dystrophy.
Vithana, Eranga N; Morgan, Patricio E; Ramprasad, Vedam; Tan, Donald T H; Yong, Victor H K; Venkataraman, Divya; Venkatraman, Anandalakshmi; Yam, Gary H F; Nagasamy, Soumittra; Law, Ricky W K; Rajagopal, Rama; Pang, Chi P; Kumaramanickevel, Govindsamy; Casey, Joseph R; Aung, Tin.
  • Vithana EN; Singapore Eye Research Institute, 11 Third Hospital Avenue, Singapore 168751, Singapore. evithana@yahoo.co.uk
Hum Mol Genet ; 17(5): 656-66, 2008 Mar 01.
Article en En | MEDLINE | ID: mdl-18024964
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Banco de datos: MEDLINE Asunto principal: Distrofia Endotelial de Fuchs / Eliminación de Gen / Antiportadores / Mutación Missense / Proteínas de Transporte de Anión Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Año: 2008 Tipo del documento: Article
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PubMed Links

Banco de datos: MEDLINE Asunto principal: Distrofia Endotelial de Fuchs / Eliminación de Gen / Antiportadores / Mutación Missense / Proteínas de Transporte de Anión Tipo de estudio: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Año: 2008 Tipo del documento: Article