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Hereditary Retinopathies
Humphries, Peter; Humphries, Marian M.; Tam, Lawrence C.S.; Farrar, G. Jane; Kenna, Paul F.; Campbell, Matthew; Kiang, Anna-Sophia
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Description for Hereditary Retinopathies
Paperback. 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. Series: Springerbriefs in Genetics. Num Pages: 46 pages, 3 black & white illustrations, 5 colour illustrations, biography. BIC Classification: MFN; MJCG1; MJQ. Category: (P) Professional & Vocational. Dimension: 237 x 157 x 10. Weight in Grams: 110.
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. ... Read more
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. ... Read more
Product Details
Format
Paperback
Publication date
2012
Publisher
Springer-Verlag New York Inc. United States
Number of pages
46
Condition
New
Series
Springerbriefs in Genetics
Number of Pages
46
Place of Publication
New York, NY, United States
ISBN
9781461444985
SKU
V9781461444985
Shipping Time
Usually ships in 15 to 20 working days
Ref
99-15
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