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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V301:
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Produktdetails
Weitere Autoren: Humphries, Marian M. / Tam, Lawrence C. / Farrar, G. Jane / Kenna, Paul F. / Campbell, Matthew
- ISBN: 978-1-4614-4498-5
- EAN: 9781461444985
- Produktnummer: 13164782
- Verlag: Springer-Verlag GmbH
- Sprache: Englisch
- Erscheinungsjahr: 2012
- Seitenangabe: 45 S.
- Masse: H23.5 cm x B15.5 cm x D0.3 cm 102 g
- Abbildungen: Book; 3 schwarz-weiße und 5 farbige Abbildungen
- Reihenbandnummer: 1
- Gewicht: 102
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