Hereditary retinopathies : progress in development of genetic and molecular therapies / Pete Humphries ...[et al.]
Humphries, Pete
(Springer, 2012)
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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. |
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No. Panggil | No. Barkod | Ketersediaan |
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e20401540 | TERSEDIA |
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