Assessment of gene mutations causing retinal degeneration / Reem Mahmoud Mohamed Mebed ; Supervised Mahmoud Ahmed Amer , Ahmed Mohamed Osman , Nahed Solouma

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Reem Mahmoud Mohamed Mebed

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TextLanguage: English Publication details: Cairo : Reem Mahmoud Mohamed Mebed , 2010Description: 71P. : charts , facsimiles ; 25cmOther title:

دراسة الطفرات الجينية المسببة لمرضى الضمور الشبكى [Added title page title]

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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Science - Department of Zoology Summary: The inherited retinal degenerative diseases are a genetically and phenotypic-ally diverse group of inherited diseases that leads to visual impairment . Retinitis pigmentosa ( RP ) is a major cause of progressive retinal disease . It was found that the rhodopsin gene ( RHO ) represents one of the causative genes for autosomal dominant RP as well as rare cases of autosomal recessive RP

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Item type	Current library	Home library	Call number	Copy number	Status	Date due	Barcode
Thesis	قاعة الرسائل الجامعية - الدور الاول	المكتبة المركزبة الجديدة - جامعة القاهرة	Cai01.12.21.M.Sc.2010.Re.A (Browse shelf(Opens below))		Not for loan		01010110054430000
CD - Rom	مخـــزن الرســائل الجـــامعية - البدروم	المكتبة المركزبة الجديدة - جامعة القاهرة	Cai01.12.21.M.Sc.2010.Re.A (Browse shelf(Opens below))	54430.CD	Not for loan		01020110054430000

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Thesis (M.Sc.) - Cairo University - Faculty of Science - Department of Zoology

The inherited retinal degenerative diseases are a genetically and phenotypic-ally diverse group of inherited diseases that leads to visual impairment . Retinitis pigmentosa ( RP ) is a major cause of progressive retinal disease . It was found that the rhodopsin gene ( RHO ) represents one of the causative genes for autosomal dominant RP as well as rare cases of autosomal recessive RP

Issued also as CD

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