Clinical course of cone dystrophy caused by mutations in the RPGR gene

BACKGROUND: Mutations in the RPGR gene predominantly cause rod photoreceptor disorders with a large variability in clinical course. In this report, we describe two families with mutations in this gene and cone involvement. METHODS: We investigated an X-linked cone dystrophy family (1) with 25 affect...

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Detalles Bibliográficos
Autores principales: Thiadens, Alberta A. H. J., Soerjoesing, Gyan G., Florijn, Ralph J., Tjiam, A. G., den Hollander, Anneke I., van den Born, L. Ingeborgh, Riemslag, Frans C., Bergen, Arthur A. B., Klaver, Caroline C. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3178018/
https://www.ncbi.nlm.nih.gov/pubmed/21866333
http://dx.doi.org/10.1007/s00417-011-1789-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3178018/
https://www.ncbi.nlm.nih.gov/pubmed/21866333
http://dx.doi.org/10.1007/s00417-011-1789-3

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