Molecular screening of the CYP4V2 gene in Bietti crystalline dystrophy that is associated with choroidal neovascularization

PURPOSE: Bietti crystalline dystrophy (BCD) is an autosomal recessive disease characterized by intraretinal deposits of multiple small crystals, with or without associated crystal deposits in the cornea. The disease is caused by mutation in the cytochrome p450, family 4, subfamily v, polypeptide 2 (...

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Detalles Bibliográficos
Autores principales: Mamatha, Gandra, Umashankar, Vetrivel, Kasinathan, Nachiappan, Krishnan, Tandava, Sathyabaarathi, Ravichandran, Karthiyayini, Thirumalai, Amali, John, Rao, Chetan, Madhavan, Jagadeesan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3154135/
https://www.ncbi.nlm.nih.gov/pubmed/21850171

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3154135/
https://www.ncbi.nlm.nih.gov/pubmed/21850171

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