Identification of differentially regulated proteins in a patient with Leber's Congenital Amaurosis – a proteomic study

BACKGROUND: To identify the pattern of protein expression in the retina from a patient with Leber's Congenital Amaurosis (LCA) secondary to a mutation in the AIPL1 gene. The retina from one eye of a patient with LCA and 7 control eyes were studied. The tissue was subjected to high resolution tw...

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Detalles Bibliográficos
Autores principales: Vorum, Henrik, Østergaard, Morten, Rice, Greg E, Honoré, Bent, Bek, Toke
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1821315/
https://www.ncbi.nlm.nih.gov/pubmed/17326818
http://dx.doi.org/10.1186/1477-5956-5-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1821315/
https://www.ncbi.nlm.nih.gov/pubmed/17326818
http://dx.doi.org/10.1186/1477-5956-5-5

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