Investigation of SLA4A3 as a candidate gene for human retinal disease

SLC4A3 has been shown to cause retinal degeneration in a genetically engineered knockout mouse, and in a naturally occurring form of canine progressive retinal atrophy considered to be the equivalent of retinitis pigmentosa in humans (RP). This study was undertaken to investigate if SLC4A3 coding va...

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Detalles Bibliográficos
Autores principales: Downs, Louise M., Webster, Andrew R., Moore, Anthony T., Michaelides, Michel, Ali, Robin R., Hardcastle, Alison J., Mellersh, Cathryn S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Brief Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876561/
https://www.ncbi.nlm.nih.gov/pubmed/27211793
http://dx.doi.org/10.1186/s12952-016-0054-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876561/
https://www.ncbi.nlm.nih.gov/pubmed/27211793
http://dx.doi.org/10.1186/s12952-016-0054-z

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