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Titlebook: Hereditary Retinopathies; Progress in Developm Pete Humphries,Marian M. Humphries,Anna-Sophia Kia Book 2012 The Author(s) 2012 gene therapy

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發(fā)表于 2025-3-21 16:34:37 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱(chēng)Hereditary Retinopathies
副標(biāo)題Progress in Developm
編輯Pete Humphries,Marian M. Humphries,Anna-Sophia Kia
視頻videohttp://file.papertrans.cn/426/425847/425847.mp4
概述Provides a snap-shot of current gene and drug-based therapies for hereditary retinal disorders.The authors explore emerging topics such as novel gene or drug delivery methods to the retina and retinal
叢書(shū)名稱(chēng)SpringerBriefs in Genetics
圖書(shū)封面Titlebook: Hereditary Retinopathies; Progress in Developm Pete Humphries,Marian M. Humphries,Anna-Sophia Kia Book 2012 The Author(s) 2012 gene therapy
描述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.
出版日期Book 2012
關(guān)鍵詞gene therapy
版次1
doihttps://doi.org/10.1007/978-1-4614-4499-2
isbn_softcover978-1-4614-4498-5
isbn_ebook978-1-4614-4499-2Series ISSN 2191-5563 Series E-ISSN 2191-5571
issn_series 2191-5563
copyrightThe Author(s) 2012
The information of publication is updating

書(shū)目名稱(chēng)Hereditary Retinopathies影響因子(影響力)




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沙發(fā)
發(fā)表于 2025-3-21 21:36:10 | 只看該作者
Pete Humphries,Marian M. Humphries,Lawrence C. S. Tam,G. Jane Farrar,Paul F. Kenna,Matthew Campbell,htungen / Messungen ausdrücken, .2. die eine . oder Variabilit?t in den Beobachtungen / Messungen erfassen, .3. die die . bzw. das Profil der (H?ufigkeits-) Verteilung beschreiben und .4. die weitere spezielle Aspekte, z.B. den . oder eine . zwischen zwei Beobachtungsreihen, untersuchen.
板凳
發(fā)表于 2025-3-22 02:35:05 | 只看該作者
地板
發(fā)表于 2025-3-22 05:05:35 | 只看該作者
5#
發(fā)表于 2025-3-22 09:34:59 | 只看該作者
Pete Humphries,Marian M. Humphries,Anna-Sophia KiaProvides a snap-shot of current gene and drug-based therapies for hereditary retinal disorders.The authors explore emerging topics such as novel gene or drug delivery methods to the retina and retinal
6#
發(fā)表于 2025-3-22 15:17:40 | 只看該作者
7#
發(fā)表于 2025-3-22 17:36:34 | 只看該作者
Introduction,itis pigmentosa is the most prevalent cause of registered visual handicap among those of working age in developed countries, while Leber congenital amaurosis is the most prevalent congenital cause of registered visual handicap.
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發(fā)表于 2025-3-22 23:18:58 | 只看該作者
Book 2012ap 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 recessiv
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發(fā)表于 2025-3-23 02:36:57 | 只看該作者
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發(fā)表于 2025-3-23 07:55:04 | 只看該作者
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