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
| 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) |
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| Format: | Electronic
eBook
|
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| Language: | English |
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| Published: |
New York, NY :
Springer New York : Imprint: Springer,
2012.
|
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| Series: | SpringerBriefs in Genetics,
1
|
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| Subjects: | |
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| Online Access: | Full Text via HEAL-Link
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