Analisis Genetik Molekul Pesakit Sindrom Fragile X Di Hospital Universiti Sains Malaysia (HUSM)[RJ506.F73 R788 2006 f rb].
Sindrom Fragile X merupakan salah satu penyakit pewarisan yang paling kerap menyebabkan keadaan kerencatan akal. Penyakit ini berlaku disebabkan oleh peningkatan jujukan trinukleotida ulangan (CGG) yang terletak dalam kawasan 5’ UTR gen FMR1 dan mengakibatkan perencatan fungsi gen ini. Fragile X...
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| Format: | Thesis |
| Language: | English |
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2006
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| Online Access: | http://eprints.usm.my/8366/ http://eprints.usm.my/8366/1/ANALISIS_GENETIK_MOLEKUL_PESAKIT_SINDROM_FRAGILE_X_DI_HOSPITAL.pdf |
| _version_ | 1848870473437282304 |
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| author | Sidek, Mohamad Ros |
| author_facet | Sidek, Mohamad Ros |
| author_sort | Sidek, Mohamad Ros |
| building | USM Institutional Repository |
| collection | Online Access |
| description | Sindrom Fragile X merupakan salah satu penyakit pewarisan yang paling kerap menyebabkan keadaan kerencatan akal. Penyakit ini berlaku disebabkan oleh peningkatan jujukan trinukleotida ulangan (CGG) yang terletak dalam kawasan 5’
UTR gen FMR1 dan mengakibatkan perencatan fungsi gen ini.
Fragile X syndrome is one of the most common inherited genetic disorders that cause mental retardation. This disease results from the expansion of a trinucleotide repeat
(CGG)n sequences, located in the 5' UTR of FMR1 gene, that further inactivate the normal function of this gene.
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| first_indexed | 2025-11-15T15:24:44Z |
| format | Thesis |
| id | usm-8366 |
| institution | Universiti Sains Malaysia |
| institution_category | Local University |
| language | English |
| last_indexed | 2025-11-15T15:24:44Z |
| publishDate | 2006 |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | usm-83662017-05-15T04:43:38Z http://eprints.usm.my/8366/ Analisis Genetik Molekul Pesakit Sindrom Fragile X Di Hospital Universiti Sains Malaysia (HUSM)[RJ506.F73 R788 2006 f rb]. Sidek, Mohamad Ros RJ370-550 Diseases of children and adolescents Sindrom Fragile X merupakan salah satu penyakit pewarisan yang paling kerap menyebabkan keadaan kerencatan akal. Penyakit ini berlaku disebabkan oleh peningkatan jujukan trinukleotida ulangan (CGG) yang terletak dalam kawasan 5’ UTR gen FMR1 dan mengakibatkan perencatan fungsi gen ini. Fragile X syndrome is one of the most common inherited genetic disorders that cause mental retardation. This disease results from the expansion of a trinucleotide repeat (CGG)n sequences, located in the 5' UTR of FMR1 gene, that further inactivate the normal function of this gene. 2006 Thesis NonPeerReviewed application/pdf en http://eprints.usm.my/8366/1/ANALISIS_GENETIK_MOLEKUL_PESAKIT_SINDROM_FRAGILE_X_DI_HOSPITAL.pdf Sidek, Mohamad Ros (2006) Analisis Genetik Molekul Pesakit Sindrom Fragile X Di Hospital Universiti Sains Malaysia (HUSM)[RJ506.F73 R788 2006 f rb]. Masters thesis, Universiti Sains Malaysia. |
| spellingShingle | RJ370-550 Diseases of children and adolescents Sidek, Mohamad Ros Analisis Genetik Molekul Pesakit Sindrom Fragile X Di Hospital Universiti Sains Malaysia (HUSM)[RJ506.F73 R788 2006 f rb]. |
| title | Analisis Genetik Molekul Pesakit Sindrom Fragile X Di Hospital Universiti Sains Malaysia (HUSM)[RJ506.F73 R788 2006 f rb]. |
| title_full | Analisis Genetik Molekul Pesakit Sindrom Fragile X Di Hospital Universiti Sains Malaysia (HUSM)[RJ506.F73 R788 2006 f rb]. |
| title_fullStr | Analisis Genetik Molekul Pesakit Sindrom Fragile X Di Hospital Universiti Sains Malaysia (HUSM)[RJ506.F73 R788 2006 f rb]. |
| title_full_unstemmed | Analisis Genetik Molekul Pesakit Sindrom Fragile X Di Hospital Universiti Sains Malaysia (HUSM)[RJ506.F73 R788 2006 f rb]. |
| title_short | Analisis Genetik Molekul Pesakit Sindrom Fragile X Di Hospital Universiti Sains Malaysia (HUSM)[RJ506.F73 R788 2006 f rb]. |
| title_sort | analisis genetik molekul pesakit sindrom fragile x di hospital universiti sains malaysia (husm)[rj506.f73 r788 2006 f rb]. |
| topic | RJ370-550 Diseases of children and adolescents |
| url | http://eprints.usm.my/8366/ http://eprints.usm.my/8366/1/ANALISIS_GENETIK_MOLEKUL_PESAKIT_SINDROM_FRAGILE_X_DI_HOSPITAL.pdf |