Physiological and molecular study of autosomal dominant neurodegenerative diseases : Huntington's disease and spinocerebellar ataxias in Egyptian patients / Nahla Nagah Eldin Ibrahim ; Supervised Said M. Rawi , Alice K. Abdelaleem , Nermeen A. Kishk

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Nahla Nagah Eldin Ibrahim

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TextLanguage: English Publication details: Cairo : Nahla Nagah Eldin Ibrahim , 2010Description: 178P. : charts, facsimiles ; 25cmOther title:

دراسة فسيولوجية وجزيئية لأمراض تحلل المخ ذات الصفة السائدة : مرض هنتينجتون وأمراض الترنح الشوكى المخيخى فى المرضى المصريين [Added title page title]

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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Science - Department of Zoology Summary: Huntington's disease (HD) and spinocerebellar ataxias are autosomal dominant neurodegenerative diseases that elicit several pathological symptoms including movement abnormalities cognitive and behavioral impairments . It was revealed that all genes associated with these genetic disorders contain CAG repeats in their coding region whose expansions are the major cause of disease progression

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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.Na.P (Browse shelf(Opens below))		Not for loan		01010110054428000
CD - Rom	مخـــزن الرســائل الجـــامعية - البدروم	المكتبة المركزبة الجديدة - جامعة القاهرة	Cai01.12.21.M.Sc.2010.Na.P (Browse shelf(Opens below))	54428.CD	Not for loan		01020110054428000

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

Huntington's disease (HD) and spinocerebellar ataxias are autosomal dominant neurodegenerative diseases that elicit several pathological symptoms including movement abnormalities cognitive and behavioral impairments . It was revealed that all genes associated with these genetic disorders contain CAG repeats in their coding region whose expansions are the major cause of disease progression

Issued also as CD

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