| 000 | 01876cam a2200325 a 4500 | ||
|---|---|---|---|
| 003 | EG-GiCUC | ||
| 008 | 110104s2010 ua dh f m 000 0 eng d | ||
| 040 |
_aEG-GiCUC _beng _cEG-GiCUC |
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| 041 | 0 | _aeng | |
| 049 | _aDeposite | ||
| 097 | _aM.Sc | ||
| 099 | _aCai01.12.21.M.Sc.2010.Na.P | ||
| 100 | 0 | _aNahla Nagah Eldin Ibrahim | |
| 245 | 1 | 0 |
_aPhysiological and molecular study of autosomal dominant neurodegenerative diseases : _bHuntington's disease and spinocerebellar ataxias in Egyptian patients / _cNahla Nagah Eldin Ibrahim ; Supervised Said M. Rawi , Alice K. Abdelaleem , Nermeen A. Kishk |
| 246 | 1 | 5 |
_aدراسة فسيولوجية وجزيئية لأمراض تحلل المخ ذات الصفة السائدة : _bمرض هنتينجتون وأمراض الترنح الشوكى المخيخى فى المرضى المصريين |
| 260 |
_aCairo : _bNahla Nagah Eldin Ibrahim , _c2010 |
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| 300 |
_a178P. : _bcharts, facsimiles ; _c25cm |
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| 502 | _aThesis (M.Sc.) - Cairo University - Faculty of Science - Department of Zoology | ||
| 520 | _aHuntington'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 | ||
| 530 | _aIssued also as CD | ||
| 653 | 4 | _aAutosomal dominant dominant spinocerebella ataxia | |
| 653 | 4 | _aHuntington's disease | |
| 653 | 4 | _aPolymerase chain reaction | |
| 700 | 0 |
_aAlice Kamal Abdelaleem , _eSupervisor |
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| 700 | 0 |
_aNermeen Adel Kishk , _eSupervisor |
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| 700 | 0 |
_aSaid Mohamed Rawi , _eSupervisor |
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| 905 |
_aNazla _eRevisor |
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| 905 |
_aSoheir _eCataloger |
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| 942 |
_2ddc _cTH |
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| 999 |
_c32506 _d32506 |
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