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Hereditary Retinopathies Progress in Development of Genetic and Molecular Therapies /

The hereditary retinopathy, retinitis pigmentosa (RP), which affects 1 in 3,500 people worldwide, is the most common cause of registered visual handicap among those of the working age in developed countries. RP is a highly variable disorder where patients may develop symptomatic visual loss in early...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Autores principales: Humphries, Pete (Autor), Humphries, Marian M. (Autor), Tam, Lawrence C. S. (Autor), Farrar, G. Jane (Autor), Kenna, Paul F. (Autor), Campbell, Matthew (Autor), Kiang, Anna-Sophia (Autor)
Autor Corporativo: SpringerLink (Online service)
Formato: Electrónico eBook
Idioma:Inglés
Publicado: New York, NY : Springer New York : Imprint: Springer, 2012.
Edición:1st ed. 2012.
Colección:SpringerBriefs in Genetics, 1
Temas:
Acceso en línea:Texto Completo