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 childhood, while others may remain asymptomatic until mid-adulthood. Most cases of RP segregate in autosomal dominant, recessive or X-linked recessive modes, with approximately 41 genes being implicated in disease pathology to date (RetNet). The extensive genetic heterogeneity associated with autosomal dominant RP (adRP) is an undisputed hindrance…
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Produktdetails
Weitere Autoren: Humphries, Marian / Tam, Lawrence C. S. / Farrar, Jane G. / Kenna, Paul F. / Campbell, Matthew
- ISBN: 978-1-4614-4499-2
- EAN: 9781461444992
- Produktnummer: 19028999
- Verlag: Springer-Verlag GmbH
- Sprache: Englisch
- Erscheinungsjahr: 2012
- Seitenangabe: 46 S.
- Plattform: PDF
- Masse: 1'099 KB
- Auflage: 2012
- Abbildungen: 3 schwarz-weiße und 5 farbige Abbildungen, Bibliographie
- Reihenbandnummer: 1
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