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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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Bibliographic Details
Call Number:Libro Electrónico
Main Authors: Humphries, Pete (Author), Humphries, Marian M. (Author), Tam, Lawrence C. S. (Author), Farrar, G. Jane (Author), Kenna, Paul F. (Author), Campbell, Matthew (Author), Kiang, Anna-Sophia (Author)
Corporate Author: SpringerLink (Online service)
Format: Electronic eBook
Language:Inglés
Published: New York, NY : Springer New York : Imprint: Springer, 2012.
Edition:1st ed. 2012.
Series:SpringerBriefs in Genetics, 1
Subjects:
Online Access:Texto Completo
Table of Contents:
  • Preface
  • Introduction
  • Gene-based Medicines directly targeting genetic defects and molecular pathologies common to multiple forms of disease
  • Molecular Medicines.