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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my-usm-ep.83662017-05-15T04:43:38Z Analisis Genetik Molekul Pesakit Sindrom Fragile X Di Hospital Universiti Sains Malaysia (HUSM)[RJ506.F73 R788 2006 f rb]. 2006 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 http://eprints.usm.my/8366/ http://eprints.usm.my/8366/1/ANALISIS_GENETIK_MOLEKUL_PESAKIT_SINDROM_FRAGILE_X_DI_HOSPITAL.pdf application/pdf en public masters Universiti Sains Malaysia Pusat Pengajian Sains Perubatan |
| institution |
Universiti Sains Malaysia |
| collection |
USM Institutional Repository |
| language |
English |
| topic |
RJ370-550 Diseases of children and adolescents |
| 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]. |
| 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.
|
| format |
Thesis |
| qualification_level |
Master's degree |
| author |
Sidek, Mohamad Ros |
| author_facet |
Sidek, Mohamad Ros |
| author_sort |
Sidek, Mohamad Ros |
| title |
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_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_sort |
analisis genetik molekul pesakit sindrom fragile x di hospital universiti sains malaysia (husm)[rj506.f73 r788 2006 f rb]. |
| granting_institution |
Universiti Sains Malaysia |
| granting_department |
Pusat Pengajian Sains Perubatan |
| publishDate |
2006 |
| url |
http://eprints.usm.my/8366/1/ANALISIS_GENETIK_MOLEKUL_PESAKIT_SINDROM_FRAGILE_X_DI_HOSPITAL.pdf |
| _version_ |
1747819710101061632 |