Noncoding variation of the gene for ferritin light chain in hereditary and age-related cataract

PURPOSE: Cataract is a clinically and genetically heterogeneous disorder of the ocular lens and an important cause of visual impairment. The aim of this study was to map and identify the gene underlying autosomal dominant cataract segregating in a four-generation family, determine the lens expressio...

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Detalles Bibliográficos
Autores principales: Bennett, Thomas M., Maraini, Giovanni, Jin, Chongfei, Sun, Wenmin, Hejtmancik, J. Fielding, Shiels, Alan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3626299/
https://www.ncbi.nlm.nih.gov/pubmed/23592921

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3626299/
https://www.ncbi.nlm.nih.gov/pubmed/23592921

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