Hereditary Retinopathies

Name: Hereditary Retinopathies
SKU: 20306379
Price: 149.00 NZD
Availability: InStock

Progress in Development of Genetic and Molecular Therapies

By:

Format:

Paperback / softback

Series:

Springerbriefs in Genetics

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Description

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 to the development of genetically based therapeutics.

Release date NZ

August 4th, 2012

Author

Audience

Professional & Vocational

Illustrations

5 Illustrations, color; 3 Illustrations, black and white; VII, 46 p. 8 illus., 5 illus. in color.

Pages

Series

Springerbriefs in Genetics

Dimensions

155x235x5

ISBN-13

9781461444985

Product ID

20306379

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