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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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Autors principals: Humphries, Pete. (Autor, http://id.loc.gov/vocabulary/relators/aut), Humphries, Marian M. (http://id.loc.gov/vocabulary/relators/aut), Tam, Lawrence C. S. (http://id.loc.gov/vocabulary/relators/aut), Farrar, G. Jane. (http://id.loc.gov/vocabulary/relators/aut), Kenna, Paul F. (http://id.loc.gov/vocabulary/relators/aut), Campbell, Matthew. (http://id.loc.gov/vocabulary/relators/aut), Kiang, Anna-Sophia. (http://id.loc.gov/vocabulary/relators/aut)
Autor corporatiu: SpringerLink (Online service)
Format: Electrònic eBook
Idioma:English
Publicat: New York, NY : Springer New York : Imprint: Springer, 2012.
Edició:1st ed. 2012.
Periòdiques:SpringerBriefs in Genetics, 1
Matèries:
Human genetics.
Gene therapy.
Ophthalmology.
Human Genetics.
Gene Therapy.
Accés en línia:https://doi.org/10.1007/978-1-4614-4499-2
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