Document Details

Document Type : Thesis 
Document Title :
physiological and molecular study of autosomal dominant neurodegenerative diseases: Huntington,s disease and spinocerebellar ataxias in
دراسة فسيولوجية وجزيئية لامراض تحلل المخ ذات الصفة السائدة: مرض هنتينجتون وامراض الترنح الشوكي المخيخي في المرضى المصريين
 
Subject : Genetic studies on Egyptian patients with neurodegerative diseases 
Document Language : English 
Abstract : أHuntington,s disese (HD) and spinocerebellar ataxias are autosomal dominant neurodegerative disease that elicit several pathological symptoms including movement abnormalities, cognitive and behavioral impairments. It was revealed that all genes associated with these genetic diorders contain GAG repeats in their coding region whose expansions are the major cause of disease progression. 
Supervisor : Sayed Mohamed Rawi 
Thesis Type : Master Thesis 
Publishing Year : 1431 AH
2010 AD 
Number Of Pages : 180 
Added Date : Wednesday, January 5, 2011 

Researchers

Researcher Name (Arabic)Researcher Name (English)Researcher TypeDr GradeEmail
سيد محمد راويRawi, sayed mohamedInvestigatorDoctoraterawisayed@yahoo.com

Files

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 28474.pdf pdf 

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